zurück

Nach Alphabet

Erkrankung Gen OMIM Dauer in Wochen
Faktor 10-Mangel*      
EXOSC9 EXOSC9 NULL
arrhythmogene ventrikuläre Kardiomyopathie, rechts JUP JUP 4-5
Arthrogrypose MYH3 MYH3 6-8
Arthrogrypose SYNE1 SYNE1 4-6
Arthrogrypose TPM2 TPM2 3-4
Arthrogrypose MYH2 MYH2 6-8
KCNC3 KCNC3 NULL
Typ 1 ACTB ACTB 2-4
Typ 2 ACTG1 ACTG1 2-4
Chimerismus 4-5
NULL
APOA5, APOC2, GPIHBP1, LMF1, LPL APOA5, APOC2, GPIHBP1, LMF1, LPL NULL
CINCA-Syndrom CIAS1 / NLRP3 CIAS1 / NLRP3 3-4
CINCA-Syndrom CIAS1 / NLRP3 CIAS1 / NLRP3 3-4
CTSF CTSF NULL
- ABCC8 ABCC8 2-4
- EIF2AK3 EIF2AK3 2-4
- GCK GCK 2-4
- INS INS 2-4
- INS INS 2-4
- KCNJ11 KCNJ11 2-4
Dermatospraxis Typ ADAMTS2 ADAMTS2 2-4
hypermobiler Typ TNXB TNXB 2-4
hypermobiler Typ TNXB TNXB 2-4
hypermobiler Typ TNXB TNXB 2-4
muskulo-kontrakturaler Typ CHST14 CHST14 2-4
NGS ADAMTS2, B4GALT7, CHST14, COL1A1, COL1A2, COL3A1, ADAMTS2, B4GALT7, CHST14, COL1A1, COL1A2, COL3A1, 4-6
progeroider Typ B3GALT6 B3GALT6 2-4
Typ 1 COL5A1 COL5A1 2-4
Typ 1 COL5A2 COL5A2 2-4
Typ 2 COL5A1 COL5A1 2-4
Typ 2 COL5A2 COL5A2 2-4
Typ 6 PLOD1 PLOD1 2-4
Typ 6A PLOD1 PLOD1 2-4
Typ 7A COL1A1 COL1A1 2-4
Typ 7B COL1A2 COL1A2 2-4
vasculär Typ COL3A1 COL3A1 2-4
vasculär Typ COL3A1 COL3A1 2-4
DEPDC5 DEPDC5 5-6
benigne familiäre infantile KCNQ2 KCNQ2 4-5
generalisierte, mit Fieberkrämpfen 4-8
metabolische ADSL, ALDH5A1, ALDH7A1, AMT, CLN3, DPYD, FOLR1, GAMT, GCDH, GLDC, PNPO, POLG, PPT1, SLC2A1, TPP1 ADSL,ALDH5A1, ALDH7A1, AMT, CLN3, DPYD, FOLR1, GAMT, GCDH, GLDC,PNPO,POLG,PPT1,SLC2A1,TPP1 4-8
CHD2 CHD2 NULL
Faktor 10-Mangel F10 F10 2-3
3
Folattransport-Defizienz FOLR1 FOLR1 5-7
verschiedene Gene für FRS verschiedene Gene für FRS 4-8
HIST1H1E HIST1H1E NULL
NGS DICER, FAS, POT1, PTPN11, TP53 DICER, FAS, POT1, PTPN11, TP53 4-6
Hyperinsulinismus-Hyperammonämie-Syndrom GLUD1 GLUD1 2-4
IQSEC2 IQSEC2 NULL
NGS DES, LMNA, PKP2, RYR2, CTNNA3, DSC2, DSG2, DSP, JUP, TGFB3, TMEM43, PLN DES,LMNA,PKP2,RYR2,CTNNA3,DSC2,DSG2,DSP,JUP,TGFB3,TMEM43, PLN 4-8
Kolobom PAX6 PAX6 3-4
Laron-ähnliches Syndrom STAT5B STAT5B 2-4
- LMNB2 LMNB2 2-4
- MFRP MFRP 3-4
- OTX2 OTX2 3-4
- SOX2 SOX2 3-4
mit Gliedmaßenanomalien SMOC1 SMOC1 3-4
NGS verschiedene Gene für MIOP verschiedene Gene für MIOP 4-6
Typ 7 GDF3 GDF3 3-4
- OSGEP OSGEP 2-4
- MAGI2 MAGI2 2-4
- MAGI2 MAGI2 2-4
NPHS1 NPHS1 NPHS1 2-4
NPHS2 NPHS2 NPHS2 2-4
NPHS4 WT1 WT1 1-2
diverse Gene diverse Gene 6
GTPBP2 GTPBP2 2-6
PLA2G6 + PANK2 PLA2G6 + PANK2 2-3
4-8
Typ 1, 2, 3, 4 COL1A1 COL1A1 4-6
Typ 1, 2, 3, 4 COL1A1 COL1A1 2-3
Typ 1, 2, 3, 4 COL1A1, COL1A2 COL1A1, COL1A2 4-6
Typ 2, 3, 4 COL1A2 COL1A2 4-6
Typ 2, 3, 4 COL1A2 COL1A2 4-6
Typ 5 und Typ 6 IFITM5 IFITM5 1-3
SHANK3 SHANK3 2-3
- SDHA SDHA 2-4
- SDHA SDHA 2-4
- SDHB SDHB 2-4
- SDHC SDHC 2-3
- SDHD SDHD 3-4
- TMEM127 TMEM127 3-4
NGS SDHA, SDHB, SDHC, SDHD, SDHAF2, MAX SDHA, SDHB, SDHC, SDHD, SDHAF2, MAX 4-8
familiäre progressive kardiale TRPM4 TRPM4 3-4
NGS BEST1, CA4, CRX, GUCA1B, IMPDH1, KLHL7, NR2E3, NRL, PRPF3, BEST1,CA4,CRX,GUCA1B,IMPDH1,KLHL7,NR2E3,NRL,PRPF3, 4-8
Shwachman-Diamond-Syndrom SBDS SBDS 2-4
multiple GDF5 GDF5 3-4
- EPCAM EPCAM 4-8
- EPCAM EPCAM 2-3
NULL
VHL VHL 2-4
VHL VHL 2-4
SFXN4 SFXN4 NULL
Faktor 12-Mangel*      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
Faktor 13-Mangel*      
ERIS ERIS 4-5
X-chromosomale ABCD1 ABCD1 2-4
Aicardi-Goutières-Syndrom 2 RNASEH2B RNASEH2B NULL
Aicardi-Goutières-Syndrom 3 RNASEH2C RNASEH2C NULL
Aicardi-Goutières-Syndrom 4 RNASEH2A RNASEH2A NULL
Albinismus, okulärer GPR143 GPR143 2-4
Aromatase-Mangel CYP19A1 CYP19A1 6-8
RIPK4 RIPK4 2
NULL
Carbamoyl-Philphat-Synthetase-1-Mangel CPS1 CPS1 2-4
- SLC22A5 SLC22A5 2-4
MNX1 MNX1 2-4
SLF2 SLF2 2-4
Faktor 13-Mangel F13 F13 4-6
SMCHD1 SMCHD1
CAVIN1/PTRF CAVIN1/PTRF 2-4
NGS CA5A, FBP1, PC, PCK1, PCK2 CA5A,FBP1,PC,PCK1,PCK2 4-6
Glycin-Enzephalopathie AMT AMT 3-4
Glycin-Enzephalopathie GLDC GLDC 3-4
Hypochondroplasie FGFR3 FGFR3 1-2
Hypochondroplasie FGFR3 FGFR3 3-4
SHROOM4 SHROOM4 2-4
CAV3 CAV3 2-4
AFF4 AFF4 NULL
ITPR3 ITPR3
Lesch-Nyhan-Syndrom HPRT1 HPRT1 3-4
Lesch-Nyhan-Syndrom HPRT1 HPRT1 2-3
CEBPA, FLT3-ITD, cKIT, NPM1 CEBPA, FLT3-ITD, cKIT, NPM1 NULL
NGS PLCG1, TP53, TET2, CREBBP, KMT2D/MLL2 PLCG1, TP53, TET2, CREBBP, KMT2D/MLL2 2
CDH1 CDH1
MLYCD MLYCD 2-4
Muskeldystrophie, kongenitale, Typ Ullrich COL6A2 COL6A2 2-4
MYH9-zugehörige Erkrankungen MYH9 MYH9 2-4
MYH9-zugehörige Erkrankungen MYH9 MYH9 2-4
NGS ALK, BARD1, BLM, CHEK2, FANCD2, GALNT14, KIF1B, NKAIN2, NME1, PALB2, PHOX2B/PMX2B, PINK1, TP53 ALK, BARD1, BLM, CHEK2, FANCD2, GALNT14, KIF1B, NKAIN2, NME1, PALB2, PHOX2B/PMX2B, PINK1, TP53 4-8
Autosomal-rezessiv OTOF OTOF 4-6
hereditäre motorisch-sensorische FAM134B FAM134B 4-6
AP1S3, CARD14, CECR1, ELANE, FOXD3, HAX1, IL10, IL AP1S3, CARD14, CECR1, ELANE, FOXD3, HAX1, IL10, IL 6-8
PAH PAH
Typ Schinzel WNT7A WNT7A 4-5
BMPR1A, SMAD4, PTEN BMPR1A,SMAD4,PTEN 14
NULL
Typ 1a GNAS, STX16 GNAS, STX16 2-4
Typ 1a GNAS GNAS 4-6
Typ 1a GNAS GNAS 2-4
Typ 1b GNAS GNAS 2-4
Typ 1b GNAS, STX16 GNAS, STX16 2-4
NGS 4-6
Typ 4 LRP5 LRP5 3-4
TWIST1 TWIST1 2-3
Simpson-Golabi-Behmel-Syndrom GPC3 GPC3 2-4
XYLT2 XYLT2 NULL
NGS ACVR1, EXT1, EXT2, FGFR1, GNAS, IDH1, IDH2, MET, NF1, PTPN11, SH3BP2, TREM2, TYROBP ACVR1, EXT1, EXT2, FGFR1, GNAS, IDH1, IDH2, MET, NF1, PTPN11, SH3BP2, TREM2, TYROBP 4-6
NULL
AIRE, CASP10, CASP8, FADD, FAS, FASLG, FOXP3, IL2RA, ITCH, PRKCD, STAT3, TNS3 AIRE, CASP10, CASP8, FADD, FAS, FASLG, FOXP3, IL2RA, ITCH, PRKCD, STAT3, TNS3 4-6
Typ 1 DYT1 DYT1 2-3
NULL
ADAMTS13 ADAMTS13 2-4
NGS 4-6
NGS ACVRL1, COL4A1, EFEMP2, ENG, FLNA, GDF2, NOTCH1, PKD1, SLC2A10, SMAD4, SMAD6 ACVRL1,COL4A1,EFEMP2,ENG,FLNA,GDF2,NOTCH1,PKD1,SLC2A10,SMAD4,SMAD6 4-6
Typ 2A VDR VDR 2-4
NGS AR, BMP15, BTG4, BUB1B, CBX2, C11orf80, CFTR, CLPP, CPEB1, CYP21A2, CYP11A1, DHH, EIF2B1, EIF2B2, EIF2B4, EIF2B5, EIF4ENIF1, ESR1, ESR2, F2, F5, FIGLA, FGF8, FGFR1, FOXL2, FSHB, FSHR, GNRH1, GNRHR, HARS2, HFM1, HSD17B3, HSD17B4, INHA, KHDC3L, KISS1, .... AR, BMP15, BTG4, BUB1B, CBX2, C11orf80, CFTR, CLPP, CPEB1, CYP21A2, CYP11A1, DHH, EIF2B1, EIF2B2, EI 4-6
Faktor 7-Mangel*      
CHGA CHGA NULL
FOXA2 FOXA2 NULL
RERE RERE NULL
Achondroplasie FGFR3 FGFR3 2-3
Achondroplasie FGFR3 FGFR3 2-4
- PDE6C PDE6C 3-4
6 PDE6H PDE6H 3-4
NGS CNGA3, CNGB3, GNAT2, PDE6C, ATF6 CNGA3,CNGB3,GNAT2,PDE6C,ATF6 4-6
Typ 2 CNGA3 CNGA3 3-4
Typ 3 CNGB3 CNGB3 3-4
Typ 4 GNAT2 GNAT2 3-4
PAX6, WT1, SOX2 PAX6, WT1, SOX2 2-4
Aniridie PAX6 PAX6 2-4
FLCN FLCN
- FLCN FLCN 3-4
Bloom-Syndrom BLM BLM 3-4
Bloom-Syndrom 8-10
Typ 1 FKBP10 FKBP10 2-4
NOTCH3 NOTCH3 2-4
NOTCH3 NOTCH3 2-3
2-3
verschiedene Gene für DURS verschiedene Gene für DURS 4-6
DYT25 GNAL GNAL 5-6
SCN8A SCN8A 4-5
0,5
Faktor 7-Mangel F7 F7 4-6
1-2
Glukose-Galaktose-Malabsorption SLC5A1 SLC5A1 2-4
Harlekintyp ABCA12 ABCA12 9-11
Ichthyosis congenita TGM1 TGM1 4-6
MBOAT7 MBOAT7
kongenitale LCT LCT 3-4
4-8
- CTNNA1 CTNNA1 4-8
NGS APC, CDH1, CTNNA1, DOT1L, FBXO24, INSR, MAP3K6, TP53 APC, CDH1, CTNNA1, DOT1L, FBXO24, INSR, MAP3K6, TP53 4-8
familiäre atypische IFNGR2 IFNGR2 NULL
familiäre atypische IL12B IL12B 10-12
familiäre atypische IL12RB1 IL12RB1 10-12
familiäre atypische STAT1 STAT1 5-6
NGS AMH, AMHR2, ANOS1, AR, ARMC2, AURKC, BNC2, CATSPER1, CCDC39, CFAP43, CFAP44, CFAP47, CFAP65, CFAP69, CFAP70, CFTR, CYP11B1, CYP17A1, CYP21A2, DMRT1, DNAH1, DNAH2, DNAH5, DNAH6, DNAH8, DNAH9, DNAH17, DNAJB13, DPY19L2, FANCM, FGF8, FGFR1, FSIP2, FSHB, ..... AMH, AMHR2, ANOS1, AR, ARMC2, AURKC, BNC2, CATSPER1, CCDC39, CFAP43, CFAP44, CFAP47, CFAP65, CFAP69, 4-6
URAD URAD NULL
Pantothenat-Kinase-assoziierte Neurodegeneration PANK2 PANK2 3-4
PLA2G6-assoziierte Neurodegeneration (PLAN) / infa PLA2G6 PLA2G6 3-4
Typ 2 ERCC6 ERCC6 3-4
- DNAJB11 DNAJB11 3-4
autosomal-rezessiv PKHD1 PKHD1 4-6
F2 F2 NULL
- WNK1 WNK1 2-4
- WNK4 WNK4 2-4
- WNK4 WNK4 2-4
- KLHL3 KLHL3 2-4
4-6
SCA1, SCA2, SCA3, SCA6, SCA7, SCA17 SCA1, SCA2, SCA3, SCA6, SCA7, SCA17 3-4
Typ 1 SCA1/ATXN1 SCA1/ATXN1 3-4
Typ 1 SCA1/ATXN1 SCA1/ATXN1 4-5
Typ 12 SCA12/PPP2R2B SCA12/PPP2R2B 3-4
Typ 17 TBP/SCA17 TBP/SCA17 3-4
Typ 2 ATXN2/SCA2 ATXN2/SCA2 3-4
Typ 3 ATXN3/SCA3 ATXN3/SCA3 3-4
Typ 6 CACNA1A/SCA6 CACNA1A/SCA6 3-4
Typ 7 ATXN7/SCA7 ATXN7/SCA7 3-4
Typ 8 SCA8 SCA8 4-5
POLR3A POLR3A NULL
NULL
NULL
NULL
NULL
Winchester-Syndrom MMP2 MMP2 4-6
Faktor V-Mangel      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
familiäre atypische Mykobakteriose*      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
Familiäre exsudative Retinopathie      
NEK9 NEK9 NULL
TBCD TBCD NULL
HARS2 HARS2 2-4
Autosomal-dominant, Typ 1 DIAPH3 DIAPH3 4-5
Autosomal-rezessiv, Typ 59 DFNB59 DFNB59 2-4
4-8
- GP1BA GP1BA 2-4
dominant-intermediäre, Typ B DNM2 DNM2 3-4
dominant-intermediäre, Typ D MPZ MPZ 4-5
Typ 1A PMP22 PMP22 2-3
Typ 1B MPZ MPZ 3-4
Typ 1C LITAF LITAF 3-4
Typ 1D EGR2 EGR2 3-4
Typ 1E PMP22 PMP22 3-4
Typ 2A MFN2 MFN2 3-4
Typ 2F HSPB1 HSPB1 3-4
Typ 2H GDAP1 GDAP1 3-4
Typ 2I MPZ MPZ 3-4
Typ 2J MPZ MPZ 4-5
Typ 2K GDAP1 GDAP1 3-4
Typ 2N AARS AARS NULL
Typ 2O DYNC1H1 DYNC1H1 2-4
Typ 2U MARS MARS NULL
Typ 4A GDAP1 GDAP1 3-4
Typ 4C SH3TC2 SH3TC2 3-4
Typ 4E EGR2 EGR2 3-4
Typ 4F PRX PRX 3-4
Typ 4J FIG4 FIG4 2-4
Typ 5 PRPS1 PRPS1 3-4
X-chromosomal Cx32 / GJB1 Cx32 / GJB1 3-4
NULL
Desbuquois Syndrom CANT1 CANT1 3-4
Donnai-Barrow-Syndrom LRP2 LRP2 4-6
MR1 MR1 4-5
COL6A3 COL6A3 NULL
verschiedene Gene für FEVR verschiedene Gene für FEVR 4-8
NGS BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 4-8
4-8
NGS PTCH1, SUFU PTCH1, SUFU 4-6
NGS PTCH2 PTCH2 4-6
ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 NULL
LDLRAP1 LDLRAP1 2-4
2-4 Wochen
Typ 1 TRPM6 TRPM6 2-4
IPEX-Syndrom FOXP3 FOXP3 2-4
Typ 3 DYNC2H1 DYNC2H1 4-8
NGS ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc 6-10
großzellig-anaplastisches NPM-ALK NPM-ALK NULL
NGS ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 2
NGS ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 2
Marinesco-Sjögren-Syndrom SIL1 SIL1 3-4
MITF MITF 3-4
NGS ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH 4-6
multiple intestinale Atresie TTC7A TTC7A 4-5
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 4-6
Duchenne / Becker DMD DMD 2-4
kongenitale LAMA2 LAMA2 8-10
MEN2A RET RET 3-4
MEN2A RET RET 3-4
MEN2B RET RET 3-4
NGS RET, MEN1, CDKN1B RET, MEN1, CDKN1B 4-8
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 4 CDKN1B CDKN1B 3-4
progressive externe POLG1 POLG1 4-8
progressive externe POLG1 POLG1 2-4
ACO2 ACO2 2-4
NR2F1 NR2F1 2-4
SLC25A46 SLC25A46 NULL
verschiedene Gene für OPA verschiedene Gene für OPA 4-6
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 3, autosomal-dominant OPA3 OPA3 2-4
Typ 7, autosomal-rezessiv TMEM126A TMEM126A 2-4
Typ 6 PLEKHM1 PLEKHM1 4-6
LRP5 LRP5 3-4
KCNJ18 KCNJ18 3-4
Sanjad-Sakati-Syndrom TBCE TBCE 2-3
RLIM RLIM NULL
Familiäre Hypomagnesiämie      
HMGCL HMGCL 4-6
Typ 3 CLDN16 CLDN16 2-4
Typ 5 CLDN19 CLDN19 2-4
Fundus albipunctatus RDH5 RDH5 4-6
familiäres Mittelmeerfieber3      
familiäres Mittelmeerfieber MEFV MEFV 1-2
familiäres Mittelmeerfieber MEFV MEFV 2-4
familiäres Mittelmeerfieber MEFV MEFV 2-4
familiäres Mittelmeerfieber MEFV MEFV NULL
FAMMM-Syndrom      
NEK9 NEK9 NULL
TBCD TBCD NULL
HARS2 HARS2 2-4
Autosomal-dominant, Typ 1 DIAPH3 DIAPH3 4-5
Autosomal-rezessiv, Typ 59 DFNB59 DFNB59 2-4
4-8
- GP1BA GP1BA 2-4
dominant-intermediäre, Typ B DNM2 DNM2 3-4
dominant-intermediäre, Typ D MPZ MPZ 4-5
Typ 1A PMP22 PMP22 2-3
Typ 1B MPZ MPZ 3-4
Typ 1C LITAF LITAF 3-4
Typ 1D EGR2 EGR2 3-4
Typ 1E PMP22 PMP22 3-4
Typ 2A MFN2 MFN2 3-4
Typ 2F HSPB1 HSPB1 3-4
Typ 2H GDAP1 GDAP1 3-4
Typ 2I MPZ MPZ 3-4
Typ 2J MPZ MPZ 4-5
Typ 2K GDAP1 GDAP1 3-4
Typ 2N AARS AARS NULL
Typ 2O DYNC1H1 DYNC1H1 2-4
Typ 2U MARS MARS NULL
Typ 4A GDAP1 GDAP1 3-4
Typ 4C SH3TC2 SH3TC2 3-4
Typ 4E EGR2 EGR2 3-4
Typ 4F PRX PRX 3-4
Typ 4J FIG4 FIG4 2-4
Typ 5 PRPS1 PRPS1 3-4
X-chromosomal Cx32 / GJB1 Cx32 / GJB1 3-4
NULL
Desbuquois Syndrom CANT1 CANT1 3-4
Donnai-Barrow-Syndrom LRP2 LRP2 4-6
MR1 MR1 4-5
COL6A3 COL6A3 NULL
verschiedene Gene für FEVR verschiedene Gene für FEVR 4-8
NGS BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 4-8
4-8
NGS PTCH1, SUFU PTCH1, SUFU 4-6
NGS PTCH2 PTCH2 4-6
ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 NULL
LDLRAP1 LDLRAP1 2-4
2-4 Wochen
Typ 1 TRPM6 TRPM6 2-4
IPEX-Syndrom FOXP3 FOXP3 2-4
Typ 3 DYNC2H1 DYNC2H1 4-8
NGS ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc 6-10
großzellig-anaplastisches NPM-ALK NPM-ALK NULL
NGS ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 2
NGS ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 2
Marinesco-Sjögren-Syndrom SIL1 SIL1 3-4
MITF MITF 3-4
NGS ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH 4-6
multiple intestinale Atresie TTC7A TTC7A 4-5
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 4-6
Duchenne / Becker DMD DMD 2-4
kongenitale LAMA2 LAMA2 8-10
MEN2A RET RET 3-4
MEN2A RET RET 3-4
MEN2B RET RET 3-4
NGS RET, MEN1, CDKN1B RET, MEN1, CDKN1B 4-8
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 4 CDKN1B CDKN1B 3-4
progressive externe POLG1 POLG1 4-8
progressive externe POLG1 POLG1 2-4
ACO2 ACO2 2-4
NR2F1 NR2F1 2-4
SLC25A46 SLC25A46 NULL
verschiedene Gene für OPA verschiedene Gene für OPA 4-6
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 3, autosomal-dominant OPA3 OPA3 2-4
Typ 7, autosomal-rezessiv TMEM126A TMEM126A 2-4
Typ 6 PLEKHM1 PLEKHM1 4-6
LRP5 LRP5 3-4
KCNJ18 KCNJ18 3-4
Sanjad-Sakati-Syndrom TBCE TBCE 2-3
RLIM RLIM NULL
Fanconi Anämie      
CHD4 CHD4 NULL
GOLGA2 GOLGA2 NULL
PRIMA1 PRIMA1 NULL
- GLI3 GLI3 3-5
- GLI3 GLI3 2-3
ALAD ALAD 4-8
8-12
4-6
4-6
4-6
4-6
4-6
BCKDK BCKDK 2-4
SLC19A3 SLC19A3 2-4
NGS CACNA1C, CACNA2D1, CACNB2, HCN4, KCNE3, SCN3B, SCN5A, TRPM4 und weitere CACNA1C, CACNA2D1, CACNB2, HCN4, KCNE3, SCN3B, SCN5A, TRPM4 und weitere 4-8
Typ 1 SCN5A SCN5A 4-6
Typ 4 CACNB2 CACNB2 NULL
Typ 8 HCN4 HCN4 4-8
NGS MYC, ARID1A, CCND3, CREBBP, GNA13, ID3, TP53 MYC, ARID1A, CCND3, CREBBP, GNA13, ID3, TP53 2
Börjeson-Forssman-Lehmann-Syndrom PHF6 PHF6 2-4
HTRA1 HTRA1 NULL
idiopathische UNC119 UNC119 2-4
NULL
NGS AIRE, CARD9, CLEC7A, IL17F, IL17RA, IL17RC, PTPN22, STAT1, TLR3, TRAF3IP2 AIRE, CARD9, CLEC7A, IL17F, IL17RA, IL17RC, PTPN22, STAT1, TLR3, TRAF3IP2 4-6
Typ 1 FBLN4/EFEMP2 FBLN4/EFEMP2 8-12
Typ 1 FBLN5 FBLN5 4-6
DiGeorge-Syndrom TBX1 TBX1 4-5
Doynsche Honigwabendystrophi EFEMP1 EFEMP1 3-4
ADAR ADAR 2-4
Dyskeratosis congenita DKC1 DKC1 4-6
NGS CTC1, DKC1, RTEL1, TERC, TERT, TINF2, ACD, NHP2 CTC1, DKC1, RTEL1, TERC, TERT, TINF2, ACD, NHP2 4-8
NGS B3GALT6, B3GAT3, BPNT2, CANT1, CHST3, CSGALNACT1, EXOC6B, FAM20B, FKBP14, FLNB, GZF1, KIF22, PLOD1, SLC10A7, SLC26A2, XYLT1 B3GALT6, B3GAT3, BPNT2, CANT1, CHST3, CSGALNACT1, EXOC6B, FAM20B, FKBP14, FLNB, GZF1, KIF22, PLOD1, 4-6
VLDLR VLDLR NULL
epidermolytische palmoplantare Keratose KRT9 KRT9 4-8
PCDH19 PCDH19 NULL
6-10
- FANCD1/BRCA2 FANCD1/BRCA2 4-8
FH FH 2-4
Galaktokinase-Mangel GALK1 GALK1 2-4
6-10
MCM4 MCM4 2-4
FGD Typ 1 MC2R MC2R 2-4
FGD Typ 2 MRAP MRAP 2-4
Glutaryl-CoA-Dehydrogenase-Mangel GCDH GCDH 8-12
GYG1 GYG1 2-4
RFT1 RFT1 3-6
kongenitaler PMM2, MPI, ALG6, ALG3, DPM1, MPDU1, ALG12, ALG8, ALG2, DPAGT1, ALG1, ALG9, DOLK, RFT1, DPM3, ALG11, SRD5A3, DDOST, ALG13, PGM1, DPM2, STT3A, STT3B, SSR4, ATP6V0A2, MAGT1, TUSC3, DHDDS, GMPPA, PGM3, NUS1 PMM2, MPI, ALG6, ALG3, DPM1, MPDU1, ALG12, ALG8, ALG2, DPAGT1, ALG1, ALG9, DOLK, RFT1, DPM3, ALG11, 4-8
kongenitaler B4GALT1, CCDC115, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MAN1B1, MGAT2, MOGS, SLC35A1, SLC35A2, SLC35C1, SLC39A8, ST3GAL3, TMEM165, TMEM199 B4GALT1, CCDC115, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MAN1B1, MGAT2, MOGS, SLC35A1, SLC35A2, S 4-8
kongenitaler MGAT2 MGAT2 4-8
kongenitaler ALG1, ALG11, ALG12, ALG2, ALG3, ALG6, ALG8, ALG9, DOLK, DPAGT1, DPM1, MAGT1, MPDU1, MPI, PGM1, PGM3, PMM2, RFT1, SRD5A3, TUSC3, B4GALT1, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MGAT2, MOGS, SLC35A1, SLC35A2, SLC35C1, TMEM165 ALG1, ALG11, ALG12, ALG2, ALG3, ALG6, ALG8, ALG9, DOLK, DPAGT1, DPM1, MAGT1, MPDU1, MPI, PGM1, PGM3, 4-8
kongenitaler Typ 1T PGM1 PGM1 2-4
kongenitaler, Typ 1 A PMM2 PMM2 4-8
kongenitaler, Typ 1B MPI MPI 2-4
kongenitaler, Typ 2 ALG9 ALG9 2-4
GRACILE-Syndrom BCS1L BCS1L 2-4
Gricelli-Syndrom verschiedene Gene für GS verschiedene Gene für GS 6-10
Typ 1 MYO5A MYO5A 6-10
Typ 2 RAB27A RAB27A 6-10
Typ 3 MLPH MLPH 4-8
ADAMTS3, CCBE1, CELSR1, EPHB4, FAT4, FLT4, FOXC2, GJC2, KIF11, PIEZO1, PTPN14, SOX18, VEGFC ADAMTS3, CCBE1, CELSR1, EPHB4, FAT4, FLT4, FOXC2, GJC2, KIF11, PIEZO1, PTPN14, SOX18, VEGFC 4-6 Wochen
Holocarboxylase-Synthetase-Mangel HLCS HLCS 4-5
- CETP CETP 2-4
NGS 4-6
PGAP3 PGAP3 NULL
NALCN NALCN NULL
juvenile Makuladegeneration CDH3 CDH3 4-5
Immundefizienz 47 ATP6AP1 ATP6AP1 4-8
infantile Hyperkalziurie CYP24A1 CYP24A1 2-4
ANKS4B ANKS4B 2-4
KMT2C KMT2C NULL
EHMT1 EHMT1 NULL
RNU4ATAC RNU4ATAC 6-8
letale Form FAM20C FAM20C 4-8
ROGDI ROGDI
MSH6, EPCAM MSH6, EPCAM 4-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
Typ 1 MSH2 MSH2 4-6
Typ 1 / 2 MLH1, MSH2 MLH1, MSH2 4-6
Typ 2 MLH1 MLH1 4-6
Typ 4 PMS2 PMS2 4-6
Typ 5 MSH6 MSH6 4-6
Typ 7 MLH3 MLH3 4-6
Typ 8 EPCAM EPCAM 4-8
Typ 8 EPCAM EPCAM 3-4
Laktoseintoleranz LCT LCT 1-3
- SPRED1 SPRED1 3-4
- SPRED1 SPRED1 3-4
NGS 2
hämophagozytische PRF1, STX11, UNC13D PRF1,STX11, UNC13D 2-4
hämophagozytische, Typ 2 PRF1 PRF1 4-8
hämophagozytische, Typ 3 UNC13D UNC13D 4-8
hämophagozytische, Typ 4 STX11 STX11 4-8
hämophagozytische, Typ 5 STXBP2 STXBP2 4-8
Typ cblA MMAA MMAA 2-4
Typ 1 und 2 CYB5R3 CYB5R3 2-4
Typ 1 und 2 CYB5R3 CYB5R3 4-8
TSC2, PKD1 TSC2, PKD1 2-3
NGS AARS2, ABCB7, ACAD9, ACADM, ACADS, ACADVL, ACO2, ADCK1, ADCK2, ADCK5, AFG3L2, AGK, AIFM1, AK2, APTX, ATP5F1A, ATP5F1E, ATPAF1, ATPAF2, AUH, BCS1L, BOLA3, C12orf65, C19orf12, CARS2, CHCHD10, CHKB, CLPB, CLPP, COA3, COA5, COA8, COASY, COQ10A, COQ10B, COQ2, COQ4, COQ5, COQ6, COQ7, COQ8A, COQ8B, COQ9 AARS2,ABCB7,ACAD9,ACADM,ACADS,ACADVL,ACO2,ADCK1,ADCK2,ADCK5,AFG3L2,AGK,AIFM1,AK2,APTX,ATP5F1A,ATP5F1 4-6
SLC5A8 SLC5A8 NULL
SON SON NULL
STAG2 STAG2 NULL
NQO1 NQO1 2-3
NGS 4-8
kongenitale schwere 4 G6PC3 G6PC3 4-8
NGS ELANE, G6PC3, HAX1, JAGN1, WAS ELANE, G6PC3, HAX1, JAGN1, WAS 4-8
- PLOD2 PLOD2 3-4
- SEC24D SEC24D 4-8
Typ 10 SERPINH1 SERPINH1 2-4
Typ 11 FKBP10 FKBP10 3-4
Typ 13 BMP1 BMP1 3-4
Typ 14 TMEM38B TMEM38B 3-4
Typ 15 WNT1 WNT1 3-4
Typ 6 CREB3L1 CREB3L1 4-8
Typ 6 SERPINF1 SERPINF1 3-4
Typ 7 CRTAP CRTAP 3-5
Typ 8 LEPRE1/P3H1 LEPRE1/P3H1 3-4
Typ 9 PPIB PPIB 3-4
MIPEP MIPEP NULL
mitochondrial 3-4
FLNA FLNA 4-6
TWNK TWNK 2-4
PNMT PNMT NULL
ADGRG1 ADGRG1 NULL
Porphyria cutanea tarda FECH, UROS, UROD and CPOX FECH, UROS, UROD and CPOX 2-4
Protein-S-Mangel PROS1 PROS1 4-6
NGS 4-6
Renal tubuläre Azidose, distal/proximal CA2 CA2 2-4
MECP2 MECP2 3-4
atypisches CDKL5 CDKL5 3-4
atypisches CDKL5 CDKL5 2-3
atypisches FOXG1 FOXG1 3-4
atypisches FOXG1 FOXG1 4-5
atypisches NTNG1 NTNG1 3-4
atypisches NTNG1 NTNG1 3-4
klassisches MECP2 MECP2 3-4
NGS DICER1, HRAS, NF1, PTPN11, TP53 DICER1, HRAS, NF1, PTPN11, TP53 4-6
NGS APC, CDKN1B, DICER1, FOXE1, HABP2, MEN1, NKX2-1, PRKAR1A, RET, PTEN, TP53 APC, CDKN1B, DICER1, FOXE1, HABP2, MEN1, NKX2-1, PRKAR1A, RET, PTEN, TP53 4-8
PAX3 PAX3 3-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
NGS CYP21A2, CYP17A1, CYP11B1, HSD3B2, POR, STAR CYP21A2, CYP17A1, CYP11B1, HSD3B2, POR, STAR 4-8
NGS CLPP, CYP11B1, CYP21A2, FSHR, HARS2, HNF1B, HSD17B4, LARS2, LHCGR, LHX1, NR5A1, POR, PSMC3IP, RSPO1, SOX3, SOX9, SRY, WNT4 CLPP, CYP11B1, CYP21A2, FSHR, HARS2, HNF1B, HSD17B4, LARS2, LHCGR, LHX1, NR5A1, POR, PSMC3IP, RSPO1, 4-8
MLPA-Analyse UPD(14)mat 2-4
- ANKRD26 ANKRD26 4-6
- GATA1 GATA1 4-6
NGS 4-6
- THPO THPO 4-6
NGS JAK2, MPL, THPO JAK2, MPL, THPO 4-6
PCGF2 PCGF2
Typ 1 ASS1 ASS1 4-6
Typ 2 SLC25A13 SLC25A13 4-6
Fanconi-Anämie*      
SLC9A9 SLC9A9
- BRIP1/FANCJ BRIP1/FANCJ 4-8
- FANCA FANCA 4-8
- FANCA FANCA 3-4
- FANCC FANCC 4-8
- FANCI FANCI 4-8
hromosomal breakage study 2-3
NGS BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, PALB2, SLX4, XRCC2 BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, PALB2, SLX4, XRCC2 4-8
mikrovillöse Einschluss-Krankheit MYO5B MYO5B 9-10
Morbus Meulengracht UGT1A1 UGT1A1 1-2
fazio-skapulo-humerale Muskeldystrophie* DUX4/DUX4L1 DUX4/DUX4L1 4-6
Feingold-Syndrom*      
Typ 1 MYCN MYCN 3-4
Typ 1 MYCN MYCN 2-3
Typ 2 MIR17HG MIR17HG 4-5
Fettsäure-Hydroxylase-assoziierte Neurodegeneration      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
FGFR2-Komplettsequenzierung      
Creutzfeldt-Jakob-Krankheit PRNP PRNP 2-3
FGFR2 FGFR2 4-5
FGFR3-Komplettsequenzierung      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
Fibrodysplasia ossificans progressiva* ACVR1 ACVR1 NULL
Fibula-Aplasie und komplexe Brachydaktylie1      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
fokale Epilepsie (NGS)      
NEK9 NEK9 NULL
TBCD TBCD NULL
HARS2 HARS2 2-4
Autosomal-dominant, Typ 1 DIAPH3 DIAPH3 4-5
Autosomal-rezessiv, Typ 59 DFNB59 DFNB59 2-4
4-8
- GP1BA GP1BA 2-4
dominant-intermediäre, Typ B DNM2 DNM2 3-4
dominant-intermediäre, Typ D MPZ MPZ 4-5
Typ 1A PMP22 PMP22 2-3
Typ 1B MPZ MPZ 3-4
Typ 1C LITAF LITAF 3-4
Typ 1D EGR2 EGR2 3-4
Typ 1E PMP22 PMP22 3-4
Typ 2A MFN2 MFN2 3-4
Typ 2F HSPB1 HSPB1 3-4
Typ 2H GDAP1 GDAP1 3-4
Typ 2I MPZ MPZ 3-4
Typ 2J MPZ MPZ 4-5
Typ 2K GDAP1 GDAP1 3-4
Typ 2N AARS AARS NULL
Typ 2O DYNC1H1 DYNC1H1 2-4
Typ 2U MARS MARS NULL
Typ 4A GDAP1 GDAP1 3-4
Typ 4C SH3TC2 SH3TC2 3-4
Typ 4E EGR2 EGR2 3-4
Typ 4F PRX PRX 3-4
Typ 4J FIG4 FIG4 2-4
Typ 5 PRPS1 PRPS1 3-4
X-chromosomal Cx32 / GJB1 Cx32 / GJB1 3-4
NULL
Desbuquois Syndrom CANT1 CANT1 3-4
Donnai-Barrow-Syndrom LRP2 LRP2 4-6
MR1 MR1 4-5
COL6A3 COL6A3 NULL
verschiedene Gene für FEVR verschiedene Gene für FEVR 4-8
NGS BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 BAP1, BRCA2, CDK4, CDKN2A, MC1R, MITF, PTEN, POT1, TP53 4-8
4-8
NGS PTCH1, SUFU PTCH1, SUFU 4-6
NGS PTCH2 PTCH2 4-6
ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 ARG1, ASL, ASS1, CPS1, GLUD1, MMUT, NAGS, OTA, OTC, PCCA, PCCB, SLC25A13, SLC25A15, SLC7A7 NULL
LDLRAP1 LDLRAP1 2-4
2-4 Wochen
Typ 1 TRPM6 TRPM6 2-4
IPEX-Syndrom FOXP3 FOXP3 2-4
Typ 3 DYNC2H1 DYNC2H1 4-8
NGS ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc ABCA3, CSF2RA, CSF2RB, MARS, SFTPB, NKX2-1 etc 6-10
großzellig-anaplastisches NPM-ALK NPM-ALK NULL
NGS ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 ATM, BCOR, EZH2, JAK1, JAK3, STAT5B, TET2, TP53 2
NGS ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 ARID1A, DDX3X, EP300, JAK3, MLL2/KMT2D, STAT3, TET2, TP53 2
Marinesco-Sjögren-Syndrom SIL1 SIL1 3-4
MITF MITF 3-4
NGS ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH ARSB, GALNS, GLB1, GNS, GUSB, HGSNAT, HYAL1, IDS, IDUA, NAGLU, SGSH 4-6
multiple intestinale Atresie TTC7A TTC7A 4-5
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 2-4
Duchenne / Becker DMD DMD 4-6
Duchenne / Becker DMD DMD 2-4
kongenitale LAMA2 LAMA2 8-10
MEN2A RET RET 3-4
MEN2A RET RET 3-4
MEN2B RET RET 3-4
NGS RET, MEN1, CDKN1B RET, MEN1, CDKN1B 4-8
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 1 MEN1 MEN1 3-4
Typ 4 CDKN1B CDKN1B 3-4
progressive externe POLG1 POLG1 4-8
progressive externe POLG1 POLG1 2-4
ACO2 ACO2 2-4
NR2F1 NR2F1 2-4
SLC25A46 SLC25A46 NULL
verschiedene Gene für OPA verschiedene Gene für OPA 4-6
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 1, autosomal-dominant OPA1 OPA1 2-4
Typ 3, autosomal-dominant OPA3 OPA3 2-4
Typ 7, autosomal-rezessiv TMEM126A TMEM126A 2-4
Typ 6 PLEKHM1 PLEKHM1 4-6
LRP5 LRP5 3-4
KCNJ18 KCNJ18 3-4
Sanjad-Sakati-Syndrom TBCE TBCE 2-3
RLIM RLIM NULL
Folattransport-Defizienz*      
EXOSC9 EXOSC9 NULL
arrhythmogene ventrikuläre Kardiomyopathie, rechts JUP JUP 4-5
Arthrogrypose MYH3 MYH3 6-8
Arthrogrypose SYNE1 SYNE1 4-6
Arthrogrypose TPM2 TPM2 3-4
Arthrogrypose MYH2 MYH2 6-8
KCNC3 KCNC3 NULL
Typ 1 ACTB ACTB 2-4
Typ 2 ACTG1 ACTG1 2-4
Chimerismus 4-5
NULL
APOA5, APOC2, GPIHBP1, LMF1, LPL APOA5, APOC2, GPIHBP1, LMF1, LPL NULL
CINCA-Syndrom CIAS1 / NLRP3 CIAS1 / NLRP3 3-4
CINCA-Syndrom CIAS1 / NLRP3 CIAS1 / NLRP3 3-4
CTSF CTSF NULL
- ABCC8 ABCC8 2-4
- EIF2AK3 EIF2AK3 2-4
- GCK GCK 2-4
- INS INS 2-4
- INS INS 2-4
- KCNJ11 KCNJ11 2-4
Dermatospraxis Typ ADAMTS2 ADAMTS2 2-4
hypermobiler Typ TNXB TNXB 2-4
hypermobiler Typ TNXB TNXB 2-4
hypermobiler Typ TNXB TNXB 2-4
muskulo-kontrakturaler Typ CHST14 CHST14 2-4
NGS ADAMTS2, B4GALT7, CHST14, COL1A1, COL1A2, COL3A1, ADAMTS2, B4GALT7, CHST14, COL1A1, COL1A2, COL3A1, 4-6
progeroider Typ B3GALT6 B3GALT6 2-4
Typ 1 COL5A1 COL5A1 2-4
Typ 1 COL5A2 COL5A2 2-4
Typ 2 COL5A1 COL5A1 2-4
Typ 2 COL5A2 COL5A2 2-4
Typ 6 PLOD1 PLOD1 2-4
Typ 6A PLOD1 PLOD1 2-4
Typ 7A COL1A1 COL1A1 2-4
Typ 7B COL1A2 COL1A2 2-4
vasculär Typ COL3A1 COL3A1 2-4
vasculär Typ COL3A1 COL3A1 2-4
DEPDC5 DEPDC5 5-6
benigne familiäre infantile KCNQ2 KCNQ2 4-5
generalisierte, mit Fieberkrämpfen 4-8
metabolische ADSL, ALDH5A1, ALDH7A1, AMT, CLN3, DPYD, FOLR1, GAMT, GCDH, GLDC, PNPO, POLG, PPT1, SLC2A1, TPP1 ADSL,ALDH5A1, ALDH7A1, AMT, CLN3, DPYD, FOLR1, GAMT, GCDH, GLDC,PNPO,POLG,PPT1,SLC2A1,TPP1 4-8
CHD2 CHD2 NULL
Faktor 10-Mangel F10 F10 2-3
3
Folattransport-Defizienz FOLR1 FOLR1 5-7
verschiedene Gene für FRS verschiedene Gene für FRS 4-8
HIST1H1E HIST1H1E NULL
NGS DICER, FAS, POT1, PTPN11, TP53 DICER, FAS, POT1, PTPN11, TP53 4-6
Hyperinsulinismus-Hyperammonämie-Syndrom GLUD1 GLUD1 2-4
IQSEC2 IQSEC2 NULL
NGS DES, LMNA, PKP2, RYR2, CTNNA3, DSC2, DSG2, DSP, JUP, TGFB3, TMEM43, PLN DES,LMNA,PKP2,RYR2,CTNNA3,DSC2,DSG2,DSP,JUP,TGFB3,TMEM43, PLN 4-8
Kolobom PAX6 PAX6 3-4
Laron-ähnliches Syndrom STAT5B STAT5B 2-4
- LMNB2 LMNB2 2-4
- MFRP MFRP 3-4
- OTX2 OTX2 3-4
- SOX2 SOX2 3-4
mit Gliedmaßenanomalien SMOC1 SMOC1 3-4
NGS verschiedene Gene für MIOP verschiedene Gene für MIOP 4-6
Typ 7 GDF3 GDF3 3-4
- OSGEP OSGEP 2-4
- MAGI2 MAGI2 2-4
- MAGI2 MAGI2 2-4
NPHS1 NPHS1 NPHS1 2-4
NPHS2 NPHS2 NPHS2 2-4
NPHS4 WT1 WT1 1-2
diverse Gene diverse Gene 6
GTPBP2 GTPBP2 2-6
PLA2G6 + PANK2 PLA2G6 + PANK2 2-3
4-8
Typ 1, 2, 3, 4 COL1A1 COL1A1 4-6
Typ 1, 2, 3, 4 COL1A1 COL1A1 2-3
Typ 1, 2, 3, 4 COL1A1, COL1A2 COL1A1, COL1A2 4-6
Typ 2, 3, 4 COL1A2 COL1A2 4-6
Typ 2, 3, 4 COL1A2 COL1A2 4-6
Typ 5 und Typ 6 IFITM5 IFITM5 1-3
SHANK3 SHANK3 2-3
- SDHA SDHA 2-4
- SDHA SDHA 2-4
- SDHB SDHB 2-4
- SDHC SDHC 2-3
- SDHD SDHD 3-4
- TMEM127 TMEM127 3-4
NGS SDHA, SDHB, SDHC, SDHD, SDHAF2, MAX SDHA, SDHB, SDHC, SDHD, SDHAF2, MAX 4-8
familiäre progressive kardiale TRPM4 TRPM4 3-4
NGS BEST1, CA4, CRX, GUCA1B, IMPDH1, KLHL7, NR2E3, NRL, PRPF3, BEST1,CA4,CRX,GUCA1B,IMPDH1,KLHL7,NR2E3,NRL,PRPF3, 4-8
Shwachman-Diamond-Syndrom SBDS SBDS 2-4
multiple GDF5 GDF5 3-4
- EPCAM EPCAM 4-8
- EPCAM EPCAM 2-3
NULL
VHL VHL 2-4
VHL VHL 2-4
SFXN4 SFXN4 NULL
Fragiles X-Syndrom*      
FMR1 FMR1 2-5
Fragiles X-Syndrom FMR1 FMR1 4-5
Frank-Ter Haar Syndrom      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
Fraser-Syndrom*      
Fraser-Syndrom FRAS1 FRAS1 14-16
Fraser-Syndrom FREM2 FREM2 14-16
Frasier-Syndrom3      
Duane-Syndrom HOXA1 HOXA1 4-6
Duane-Syndrom ROBO3 ROBO3 2-4
Frasier-Syndrom WT1 WT1 2-4
Friedreich Ataxie*      
adrenogenitales Syndrom CYP11B1 CYP11B1 4-6
adrenogenitales Syndrom CYP17A1 CYP17A1 4-6
adrenogenitales Syndrom CYP17A1 CYP17A1 NULL
adrenogenitales Syndrom CYP21A2 CYP21A2 2-4
adrenogenitales Syndrom CYP21A2 CYP21A2 4-5
adrenogenitales Syndrom HSD3B2 HSD3B2 4-6
adrenogenitales Syndrom STAR STAR 8-10
adrenogenitales Syndrom CYP11B1 CYP11B1 2-4
Typ 1 TYR TYR 2-4
Typ 1 GPR143, PITX2, FOXC1, TWIST GPR143, PITX2, FOXC1, TWIST 2-4
Typ 2 OCA2 OCA2 2-4
Typ 2 OCA2, TYR OCA2, TYR 2-4
Typ 2, Modifier MC1R MC1R 2-4
Typ 3 TYRP1 TYRP1 2-4
Typ 4 SLC45A2 SLC45A2 2-4
Typ 7 C10ORF11 C10ORF11 2-4
BBS1, BBS10 BBS1, BBS10 2-3
BBS1 BBS1 BBS1 3-5
BBS10 BBS10 BBS10 2-4
BBS14 CEP290 CEP290 3-5
BBS7 BBS7 BBS7 3-5
BBS9 BBS9 BBS9 3-5
CYLD CYLD 4-6
LC25A20 LC25A20 2-4
Cherubismus SH3BP2 SH3BP2 4-6
CHILD-Syndrom NSDHL NSDHL 6-8
NULL
postaxiale DHODH DHODH 2-4
ASAH1 ASAH1 2-4
Friedreich Ataxie FXN FXN 3-4
Friedreich Ataxie FXN FXN 2-4
Gliome POT1 POT1 2-4
Gliome POT1 POT1 2-4
NGS TP53, BRCA2, POT1, PTEN, MSH2, MSH6, MLH1, PMS2, CDKN2A, CDKN2B, RTEL1, TSC1, NF1, NF2 TP53, BRCA2, POT1, PTEN, MSH2, MSH6, MLH1, PMS2, CDKN2A, CDKN2B, RTEL1, TSC1, NF1, NF2 4-8
maligne RYR1, CACNA1S, STAC3 RYR1, CACNA1S,STAC3 4-6
KABUK1 MLL2/KMT2D MLL2/KMT2D 2-4
KABUK1 MLL2/KMT2D MLL2/KMT2D 2-4
KABUK2 KDM6A KDM6A 2-4
KABUK2 KDM6A KDM6A 2-4
NGS 4-6
NGS ALX4, FIG4, MSX2, RUNX2, VAC14 ALX4, FIG4, MSX2, RUNX2, VAC14 4-6
Kniest-Dysplasie COL2A1 COL2A1 4-6
Kniest-Dysplasie COL2A1 COL2A1 4-6
Kniest-Dysplasie COL2A1 COL2A1 2-3
NGS PRF1, UNC13D, STX11, STXBP2 PRF1, UNC13D, STX11, STXBP2 4-8
KCNT1 KCNT1 NULL
HNF1ß/TCF2 HNF1ß/TCF2 2-4
LHX1 LHX1 2-4
WNT4 WNT4 2-4
WNT4 WNT4 2-4
- JAK2, Exon 14, V617F JAK2, Exon 14, V617F 1-2
- JAK2 JAK2 1-2
- MPL MPL 1-2
- PDGFRB PDGFRB 3-4
- PRV1 PRV1 NULL
NGS JAK2, CALR, MPL JAK2, CALR, MPL 2
NGS JAK2, CALR, MPL, ASXL1, CBL, DNMT3A, EZH2, IDH1, IDH2, RUNX1, SF3B1, SRSF2, TET2, TP53, ZRSR2 JAK2, CALR, MPL, ASXL1, CBL, DNMT3A, EZH2, IDH1, IDH2, RUNX1, SF3B1, SRSF2, TET2, TP53, ZRSR2 2
NGS NF1, NF2, SMARCB1, SPRED1 NF1, NF2, SMARCB1, SPRED1 4-6
Typ 1 NF1 NF1 4-6
Typ 1 NF1 NF1 2-3
Typ 2 NF2 NF2 4-6
Typ 2 NF2 NF2 2-4
Typ 3 SMARCB1 SMARCB1 4-6
NGS NPC1, NPC2 NPC1, NPC2 4-8
Typ A/B SMPD1 SMPD1 2-4
Typ C1 NPC1 NPC1 4-6
Typ C2 NPC2 NPC2 4-6
Typ C2 NPC2 NPC2 4-6
NGS APC, BLM, MSH2, PALB2, RB1, RECQL4, TP53, WRN APC, BLM, MSH2, PALB2, RB1, RECQL4, TP53, WRN 4-8
Purin-Nukleosid-Phosphorylase-Mangel PNP PNP 8-10
- SMARCA4 SMARCA4 3-4
SESAME-Syndrom KCNJ10 KCNJ10 3-4
Verlangsamte Nervenleitgeschwindigkeit, autosomal- ARHGEF10 ARHGEF10 4-6
EDNRB, NRTN EDNRB, NRTN 3-4
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
KCNH1 KCNH1 NULL
Zirrhose-Dystonie-Polyzythämie-Hypermagnesiämie-Sy SLC30A10 SLC30A10 3-4
Zirrhose-Dystonie-Polyzythämie-Hypermagnesiämie-Sy SLC30A10 SLC30A10 4-5
Frontallappenepilepsie, nächtliche      
autosomal-dominante CHRNA2, CHRNA4, CHRNB2, CRH, DEPDC5, KCNT1 CHRNA2, CHRNA4, CHRNB2, CRH, DEPDC5, KCNT1 4-8
HNF1B/TCF2 HNF1B/TCF2 2-3
- HNF1B/TCF2 HNF1B/TCF2 2-4
Fruktoseintoleranz, hereditär      
ATAD3B ATAD3B 2-4
CDK13 CDK13 NULL
CTBP1 CTBP1 NULL
PCDH12 PCDH12 NULL
PCM1 PCM1
PTCHD1 PTCHD1 NULL
RASA1 RASA1
RREB1 RREB1 NULL
SH3TC1 SH3TC1 3-4
SHANK2 SHANK2 NULL
TANC2 TANC2 2-4
WDR91 WDR91 NULL
HMGCL HMGCL 2-4
3-Methyl-Crotonyl-CoA-Carboxylase-1-Mangel MCCC1 MCCC1 2-4
Aarskog-Syndrom FGD1 FGD1 2-4
Aarskog-Syndrom FGD1 FGD1 4-6
Abetalipoproteinämie MTP MTP 4-6
Typ 1B SLC26A2 SLC26A2 3-4
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 4-6
Typ 2 COL2A1 COL2A1 2-3
GLI3, KIF7 GLI3, KIF7 NULL
ACTH-Mangel TBX19 TBX19 2-4
ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ ARHGAP31, DLL4, DOCK6, EOGT, NOTCH1, RBPJ 4-8
ADSL ADSL 6-10
KSR2 KSR2 2-4
DYRK1B DYRK1B 2-4
- LEP LEP 2-4
- LEPR LEPR 2-4
- MC3R MC3R 2-4
- MC4R MC4R 2-4
- PCSK1 PCSK1 2-4
- POMC POMC 2-4
MLPA LEPR, MC4R, POMC, LEP, MC2R LEPR, MC4R, POMC, LEP, MC2R 2-4
NGS BBS1, BBS10, DYRK1B, KSR2, LEP, LEPR, MC3R, MC4R, NR0B2, NTRK2, PCSK1, POMC, PPARG, SIM1, UCP3 BBS1,BBS10,DYRK1B,KSR2,LEP,LEPR,MC3R,MC4R,NR0B2,NTRK2,PCSK1,POMC,PPARG,SIM1,UCP3 4-6
ADPKD PKD1, PKD2 PKD1, PKD2 2-4
Agammaglobulinämie IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 IGHM, IGLL1, CD79A, CD79B, BLNK, PIK3R1 4-6
X-chromosomal 1 BTK BTK 2-4
NGS BCKDHA, BCKDHB, DBT, DLD BCKDHA, BCKDHB, DBT, DLD 4-6
Typ 1A BCKDHA BCKDHA 2-4
Typ 1B BCKDHB BCKDHB 2-4
Typ 2 DBT DBT 2-4
NGS IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, SAMHD1, ADAR 4-8
- COL3A1 COL3A1 2-4
verschiedene Gene für ALB verschiedene Gene für ALB 4-6
GNAS GNAS 2-4
Alexander-Syndrom GFAP GFAP 4-6
Alkaptonurie HGD HGD 2-4
alpha-1-Antitrypsin-Mangel SERPINA1 SERPINA1 1-2
Alpha-Ketoglutarat-Dehydrogenase-Mangel OGDH OGDH 3-5
IGFALS IGFALS 2-4
SLC34A2 SLC34A2 2-4
Amyloidpolyneuropathie TTR TTR 2-3
Amyloidpolyneuropathie TTR TTR 2-3
SIGMAR1 SIGMAR1 NULL
SEPTIN9 SEPTIN9
PIP PIP NULL
Androgeninsensitivitäts-Syndrom AR AR 2-4
Androgeninsensitivitäts-Syndrom AR AR 2-4
SNRPN, UBE3A SNRPN,UBE3A 2-4
4-8
Sequenzierung des UBE3A-Gens UBE3A UBE3A 2-4
Angiotensin 1 konvertierendes Enzym ACE ACE 1-2
ANK3 ANK3
RSPO4 RSPO4 3-4
ANXA1-Mutation ANXA1 ANXA1 3-4
familiäres thorakales ACTA2 ACTA2 4-5
familiäres thorakales MYLK MYLK 10-11
NGS BCOR, BCORL1, DNMT3A, PIGA, ASXL1 BCOR, BCORL1, DNMT3A, PIGA, ASXL1 2-3
Apparenter Mineralocorticoid-Überschuss HSD11B2 HSD11B2 2-4
kongenitale kontrakturale FBN2 FBN2 5-6
Typ 1 VPS33B, VIPAS39 VPS33B,VIPAS39 4-6
Typ 1 VPS33B VPS33B 2-4
Typ 2 VIPAS39 VIPAS39 2-4
KARS KARS NULL
PTPRQ PTPRQ 3-6
PKHD1, DZIP1L, PKD1 PKHD1, DZIP1L, PKD1 15-16
PKHD1 PKHD1 2-4
DZIP1L DZIP1L NULL
PKHD1L1 PKHD1L1 4-6
familiäre isolierte RYR2 RYR2 2-4
der Kindheit WISP3 WISP3 2-4
ARX-assoziierte Erkrankungen ARX ARX 3-4
- MRE11A MRE11A 3-5
AFG3L2 AFG3L2 NULL
Typ 1 FLNB FLNB 2-3
Typ 1 FLNB FLNB 2-4
Typ 1 FLNB FLNB 2-4
Typ 2 SLC26A2 SLC26A2 3-4
Typ 3 FLNB FLNB 2-3
Typ 3 FLNB FLNB 3-4
Typ 3 FLNB FLNB 5-6
NLGN1 NLGN1
Typ 1 PITX2 PITX2 2-4
NGS 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
Sequenzanalyse CDKN1C CDKN1C CDKN1C 4-6
Sequenzanalyse CDKN1C CDKN1C CDKN1C 2-4
Sequenzanalyse NLRP2 NLRP2 NLRP2 2-4
4-8
- GP1BA, GP1BB, G9 GP1BA, GP1BB, G9 4-6
Typ C GP9 GP9 2-4
bikuspide Aortenklappe GATA5, NKX2-5, NOTCH1, SMAD6 GATA5, NKX2-5, NOTCH1, SMAD6 4-6
Biotinidase-Mangel BTD BTD 2-4
BTD BTD NULL
- DICER1 DICER1 4-8
- DICER1 DICER1 4-8
Bohring-Opitz-Syndrom ASXL1 ASXL1 2-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
IHH IHH 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A3 SLC52A3 2-4
Brown-Vialetto-van Laere-Syndrom SLC52A2 SLC52A2 2-4
BARD1 BARD1 2-3
BRIP1 BRIP1 2-3
- ATM ATM 4-5
- ATM ATM 4-6
- BARD1 BARD1 4-8
- BRCA1, BRCA2 BRCA1, BRCA2 4-8
- BRCA1 BRCA1 4-6
- BRCA1 BRCA1 2-3
- BRCA2 BRCA2 4-6
- BRCA2 BRCA2 2-3
- BRIP1 BRIP1 4-5
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- CHEK2 CHEK2 4-6
- NBN NBN 4-5
- PALB2 PALB2 2-4
- RAD51C RAD51C 4-5
- STK11 STK11 3-4
- STK11 STK11 3-4
MLPA PALB2, RAD50, RAD51D PALB2, RAD50, RAD51D 2-4
RAD50 RAD50
TXNL4A TXNL4A 2-4
Butyrylcholinesterase-Mangel BCHE BCHE 4-5
CACH-Syndrom EIF2B1 EIF2B1 3-4
CACH-Syndrom EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 6-8
CACH-Syndrom EIF2B2 EIF2B2 4-5
CACH-Syndrom EIF2B3 EIF2B3 4-5
CACH-Syndrom EIF2B4 EIF2B4 4-5
CACH-Syndrom EIF2B5 EIF2B5 4-5
Caffey-Krankheit COL1A1 COL1A1 4-6
Caffey-Krankheit COL1A1 COL1A1 2-3
CAMRQ-Syndrom ATP8A2 ATP8A2 4-6
Canavan-Krankheit ASPA ASPA 4-6
Typ 1 PRKAR1A PRKAR1A 4-6
DSP DSP 2-4
neuronale 4-8
Typ 1 PPT1 PPT1 5-6
Typ 1, 8, 2, 6, 3 PPT1, CLN8, TPP1, CLN6, CLN3 PPT1, CLN8, TPP1, CLN6, CLN3 3-4
Typ 2 TPP1 TPP1 10-12
Typ 3 CLN3 CLN3 10-12
Typ 3 CLN3 CLN3 10-12
Typ 5 CLN5 CLN5 NULL
Typ 6 CLN6 CLN6 3-4
Typ 7 MFSD8 MFSD8 3-4
Typ 8 CLN8 CLN8 3-4
NDRG1 NDRG1 NULL
ERF ERF NULL
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
Chloride Diarrhoe SLC26A3 SLC26A3 3-4
rhizomele, Typ 1 PEX7 PEX7 4-6
rhizomele, Typ 2 GNPAT GNPAT 4-6
rhizomele, Typ 3 AGPS AGPS 4-6
Typ 2 EBP EBP 4-8
x-chromosomal, brachytelephalangealer Typ ARSE ARSE 4-8
metaphysäre, Typ Schmid COL10A1 COL10A1 2-3
Typ Blomstrand PTH1R PTH1R NULL
Chorea Huntington HTT HTT 4-5
- NKX2-1 NKX2-1 3-4
Chorea-Akanthozytose VPS13A VPS13A 7-9
Chorioideremie CHM CHM 4-6
CHM CHM 4-6
NULL
IgVH IgVH 2-3
CHST3-assoziierte Skelettdysplasie CHST3 CHST3 2-4
CUBN, MMACHC, ABCD4, LMBRD1, MMADHC, MMUT, MTR, MTRR, HCFC1, TCN2 CUBN,MMACHC,ABCD4,LMBRD1,MMADHC,MMUT,MTR,MTRR,HCFC1, TCN2 4-6
Typ A ERCC8 ERCC8 3-4
Typ B ERCC6 ERCC6 3-4
RPS6KA3 RPS6KA3 NULL
SMARCE1 SMARCE1
4-6
VPS13B/COH1 VPS13B/COH1 4-6
VPS13B/COH1 VPS13B/COH1 2-3
RAD21 RAD21 NULL
4-6
NGS AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD AKT1, KLLN, PIK3CA, PTEN, SEC23B, SDHB, SDHD 4-6
Typ 1 PTEN PTEN 3-4
Typ 1 PTEN PTEN 2-3
Typ 1 PTEN PTEN 2-3
Typ 2 SDHB SDHB 3-4
Typ 3 SDHD SDHD 3-4
Typ 4 KLLN KLLN 3-4
Typ 5 PIK3CA PIK3CA 3-4
Typ 6 AKT1 AKT1 3-4
Typ 7 SEC23B SEC23B 3-4
SDHB SDHB 3-4
Crigler-Najjar-Syndrom UGT1A1 UGT1A1 4-5
1 CRLF1 CRLF1 3-4
Crouzon-Syndrom FGFR2 FGFR2 3-4
Crouzon-Syndrom mit Akanthose nigricans FGFR3 FGFR3 3-4
Cumarin/Warfarin-Sensitivität CYP4F2 CYP4F2 2-3
Cumarin/Warfarin-Sensitivität VKORC1 VKORC1 2-3
Cystinose CTNS CTNS 2-4
Cystinose CTNS CTNS 2-4
Typ 1 SLC3A1 und SLC7A9 SLC3A1 und SLC7A9 2-4
Typ 1 SLC3A1 SLC3A1 2-4
Typ 2 und 3 SLC7A9 SLC7A9 2-4
- CLCN5 CLCN5 2-4
- OCRL/OCRL1 OCRL/OCRL1 2-4
NGS 4-6
DSPP DSPP NULL
DES DES 2-4
Diabetes insipidus AVP, AVPR2, AQP2 AVP, AVPR2, AQP2 4-6
Diamond-Blackfan-Anämie GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 GATA1, TSR2, RPL5, RPL11, RPL35A, RPS10, RPS17, RPS19, RPS24, RPS26 4-6
Diamond-Blackfan-Anämie RPS19 RPS19 2-4
PHIP PHIP NULL
Dihydropyrimidin-Dehydrogenase-Mangel DPYD DPYD 1
FLNC FLNC NULL
DNAJC6 DNAJC6 NULL
autosomal-dominant GCH1 GCH1 2-3
autosomal-dominant GCH1 GCH1 3-4
autosomal-rezessives TH TH 2-4
autosomal-rezessives TH TH 2-4
Dravet Syndrom GABRG2 GABRG2 3-4
ROBO3 ROBO3 2-4
DYM DYM 2-4
- IKBKAP IKBKAP 3-4
Typ 6 THAP1 THAP1 4-5
4-8
Eagle-Barret-Syndrom CHRM3 CHRM3 5-6
EGFR EGFR NULL
COL5A1 COL5A1 NULL
EMD EMD 2-4
breast cancer 1
kongenitale, durch Enteropeptidase-Mangel TMPRSS15/PRSS7 TMPRSS15/PRSS7 2-4
TRRAP TRRAP
ST7 ST7 NULL
SUOX SUOX 3-5
Enzephalopathie, epileptische frühinfantile SCN2A SCN2A 6-8
FGFR1 FGFR1 NULL
- COL17A1 COL17A1 6-8
- COL7A1, KRT5 COL7A1, KRT5 2-3
dystrophe COL7A1 COL7A1 6-8
junktionale ITGB4 ITGB4 2-4
junktionale LAMA3 LAMA3 4-5
junktionale, Typ nicht-Herlitz LAMB3 LAMB3 3-4
NGS COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 COL7A1, ITGB4, LAMA3, LAMB3, LAMC2, KRT14, KRT5 4-8
Typ Herlitz LAMC2 LAMC2 3-4
HCN1 HCN1
NTRK2 NTRK2 4-6
GRIN2B GRIN2B NULL
SLC6A1 SLC6A1 NULL
6
Typ 1 und 3B KIF21A KIF21A 2-4
Typ 2 PHOX2A PHOX2A 2-4
Typ 3A TUBB3 TUBB3 4-5
NGS ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, FBLN1, FGF10, FGF16, FGF9, FGFR1, FGFR2, FGFR3, FMN1, GDF5, GDF6, GJA1, GLI3, GNAS, GREM1, GSC, HDAC4, HDAC8, HOXA11, HOXA13, HOXD13, IHH, KCNJ2, KIF7, ... ARHGAP31, BHLHA9, BMP2, BMPR1B, CDH3, CHSY1, CKAP2L, DHODH, DLL4, DLX5, DOCK6, EOGT, ESCO2, FAM58A, 4-6
Faktor 11-Mangel F11 F11 4-6
Faktor12-Mangel F12 F12 3-5
Faktor 13A1-Mangel F13A1 F13A1 4-6
Faktor V-Mangel F5 F5 3-4
familiäre atypische Mykobakteriose IFNGR1 IFNGR1 NULL
ADCY5 ADCY5 NULL
FANCA FANCA
3
FA2H FA2H 3-4
FGFR3 FGFR3 3-4
Fibula-Aplasie und komplexe Brachydaktylie GDF5 GDF5 2-4
Frank-Ter Haar Syndrom SH3PXD2B SH3PXD2B 6-8
AFF2 AFF2 NULL
ALDOB ALDOB
Fruktoseintoleranz, hereditär ALDOB ALDOB 2-4
SZT2 SZT2 NULL
1
juveniler Typ CTSA CTSA 2-4
SOX3 SOX3 2-4
Typ 1 ENPP1 ENPP1 2-4
generalisierten pustulösen Psoriasis IL36RN IL36RN 3-4
SRY SRY 2-4
NR5A1 NR5A1 2-4
- AMXY AMXY 3-4
- SRY SRY 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Gonadendysgenesie NR0B1 NR0B1 2-4
Typ 1A MYOT MYOT 2-4
Typ 2A CAPN3 CAPN3 2-4
Typ 2B DYSF DYSF 2-4
Typ 2C SGCG SGCG 2-4
Typ 2D SGCA SGCA 2-4
Typ 2E SGCB SGCB 2-4
Typ 2I FKRP FKRP 2-4
FKTN FKTN 2-4
APOL1 APOL1 3-4
4-6
Fruktose 1,6 Bisphosphatase-Mangel FBP1 FBP1 2-4
Fruktose 1,6 Bisphosphatase-Mangel ALDOB, FBP1 ALDOB, FBP1 2-4
Glucose-6-Phosphat-Dehydrogenase-Defizienz G6PD G6PD 4-6
SLC2A1 SLC2A1 3-4
SLC2A1 SLC2A1 3-4
GSTM1, GSTP1, GSTT1 GSTM1, GSTP1, GSTT1 2-3
Typ 0 GYS2 GYS2 2-4
Typ 1B/1C SLC37A4/G6PT1 SLC37A4/G6PT1 2-4
Typ 2 GAA GAA 2-4
Typ 2 GAA GAA 2-4
Typ 3b AGL AGL 2-4
Typ 4 GBE1 GBE1 2-4
Typ 5 PYGM PYGM 2-4
Typ 6 PYGL PYGL 2-4
Typ 7 PFKM PFKM 2-4
Typ 9A PHKA2 PHKA2 2-4
Typ 9B PHKB PHKB 2-4
NGS AGL, FBP1, G6PC, GAA, GBE1, PHKA2, PHKB, PHKG2, PYGM, SLC2A2, SLC37A4, ALDOA, ENO3, EPM2A, FBP2, GYG1, GYG2, GYS1, GYS2, LAMP2, LDHA, LDHB, NHLRC1, PFKL, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKG1, PRKAG2, PRKAG3, PYGL AGL,FBP1,G6PC,GAA,GBE1,PHKA2,PHKB,PHKG2,PYGM,SLC2A2,SLC37A4,ALDOA,ENO3,EPM2A,FBP2,GYG1,GYG2,GYS1,GYS 4-8
Typ 11 SLC2A2 SLC2A2 2-4
Typ 1A G6PC1/G6PC G6PC1/G6PC 2-4
Typ 1-3 GLB1 GLB1 14-16
PTCH1 PTCH1
Gray-platelet-Syndrom NBEAL2 NBEAL2 8-10
GLI3 GLI3 2-3
GRIN1 GRIN1 NULL
X-Chromosomal POU3F4 POU3F4 2-4
- BRAF BRAF 2
NGS BRAF, KLF2, CDKN1B BRAF, KLF2, CDKN1B 2
GATA3 GATA3 NULL
GATA3 GATA3 NULL
HECW2 HECW2 NULL
Prognosemarker IL-28B IL-28B 2-3
NGS ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, SLX4, XRCC2 ABCB11, AGL, APC, CDKN2A, FAH, G6PC, HMBS, PPOX, PRKAR1A, SPRTN, BRCA2, BRIP1, FANCA, FANCB, FANCC, 4-8
PMP22 PMP22 3-4
PMP22 PMP22 3-4
DNMT1 DNMT1 NULL
KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1 KCNN4, PIEZO1, SLC4A1, RHAG, RHCE, RHD, ABCB6 und SLC2A1
verschiedene Gene für HPS verschiedene Gene für HPS 4-8
Typ 1 HPS1 HPS1 2-4
Typ 3 HPS3 HPS3 2-4
Typ 5 HPS5 HPS5 2-4
Typ 6 HPS6 HPS6 2-4
Typ 8 BLOC1S3 BLOC1S3 2-4
MED13L MED13L NULL
verschiedene Gene verschiedene Gene NULL
- EDN3 EDN3 3-4
- EDNRB EDNRB 3-4
Histaminintoleranz ABP1 ABP1 4-6
Histaminintoleranz HNMT HNMT 4-5
HIV-1-Wirtsresistenz CCR5 CCR5 2-3
4-6
Holoprosenzephalie GLI2 GLI2 7-8
Holoprosenzephalie PTCH1 PTCH1 4-6
Holoprosenzephalie SHH SHH 4-6
Holoprosenzephalie SIX3 SIX3 8-9
Holoprosenzephalie TGIF TGIF 7-8
Holoprosenzephalie ZIC2 ZIC2 8-10
Holt-Oram-Syndrom TBX5 TBX5 2-4
Holt-Oram-Syndrom TBX5 TBX5 2-4
Homocysteinämie CBS CBS 4-6
- DCN DCN 2-4
- SLC4A11 SLC4A11 2-4
Hornhautdystrophie ZEB1 ZEB1 2-4
Hutchinson-Gilford-Syndrom LMNA LMNA 3-4
KYNU KYNU 5-6
X-chromosomal L1CAM L1CAM 3-5
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom DOCK8 DOCK8 4-8
Hyper-IgE-Syndrom STAT3 STAT3 4-8
Hyper-IgE-Syndrom TYK2 TYK2 4-8
NGS DOCK8, STAT3, TYK2 DOCK8, STAT3, TYK2 4-8
Hypereosinophilie-Syndrom FIP1L1, PDGFRA FIP1L1, PDGFRA 3-4
SCN4A SCN4A 3-5
CASR CASR 2-4
Typ 2 GNA11 GNA11 2-4
Typ 3 AP2S1 AP2S1 2-4
Typ1 CASR CASR 2-4
Hyperlipoproteinämie LPL LPL 2-4
Typ 3 APOE APOE 2-3
Typ 1 AGXT AGXT 2-4
Typ 1 AGXT AGXT 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 2 GRHPR GRHPR 2-4
Typ 3 HOGA1/DHDPSL HOGA1/DHDPSL 2-4
SLC26A1 SLC26A1 2-4
4-6
TRPV6 TRPV6 2-4
PIGV PIGV NULL
Typ 2 ALDH4A1 ALDH4A1 3-4
4-6
Hypoalphalipoproteinämie LCAT LCAT 2-4
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 4-6
Hypochondrogenesie COL2A1 COL2A1 2-3
AKT2 AKT2 2-4
ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1 ACAT1, CA5A, FBP1, G6PC, GYS1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, PC, PCK1, PCK2, PYGL, SLC16A1
NGS 4-8
NGS 4-6
kongenitale Katarakt FAM126A FAM126A 4-6
SLC34A3 SLC34A3 2-4
SLC34A1 SLC34A1 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
autosomal-dominant FGF23 FGF23 2-4
NGS ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 ARNT2, CDON, GLI2, HESX1, LHX3, LHX4, OTX2, POU1F1, PROP1, RBM28, SOX2, SOX3 4-8
Typ 1 LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR LHX3, LHX4, GH1, HESX1, POU1F1, PROP1, GHRHR 2-4
Typ 1 POU1F1 POU1F1 2-4
Typ 3 LHX3 LHX3 2-4
Typ 4 LHX4 LHX4 2-4
Typ 5 HESX1 HESX1 2-4
Typ 2 SLC38A8 SLC38A8 3-4
hypoplastisches Linksherz-Syndrom NKX2-5 NKX2-5 2-4
Typ 1 SLC22A12 SLC22A12 2-4
Typ 2 SLC2A9 SLC2A9 2-4
MLPA 2-4
NGS HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 HFE, HFE2/HJV, HAMP, TFR2, SLC40A1, FTL, FTH1 und BMP6 4-8
Typ 1 HFE HFE 4-8
Typ 2A HFE2/HJV HFE2/HJV 4-8
Typ 2B HAMP HAMP 4-8
Typ 3 TFR2 TFR2 4-8
Typ 4 SLC40A1 SLC40A1 2-4
Typ 5 BMP6 BMP6 4-8
Hämophilie B F9 F9 4-6
NGS ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere ABCA12, ALOX12B, ALOXE3, CYP4F22, KRT1, KRT10, LIPN, NIPAL4, STS, TGM1 und weitere 4-8
X-chromosomale STS STS 5-8
X-chromosomale STS STS 5-8
ADCY10 ADCY10 2-4
IGF1R, IGFBP3, IGFALS IGF1R, IGFBP3, IGFALS 2-4
IL3RA IL3RA 2-4
kombinierter schwerer JAK3 JAK3 4-6
kombinierter schwerer CD247, CD3D/E, CD45, CORO1A, DCLRE1C , IL2RG, IL7R CD247, CD3D/E, CD45, CORO1A, DCLRE1C ,IL2RG, IL7R 4-8
kombinierter schwerer ZAP70 ZAP70 6-8
Immundefizienz IRAK4 IRAK4 6-8
Immunglobulin A (IgA)-Mangel TNFRSF13B TNFRSF13B 4-6
ITGA2 ITGA2 2-3
DEAF1 DEAF1 NULL
CNKSR2 CNKSR2 NULL
SETD5 SETD5 NULL
Interleukin-1 Rezeptor-Antagonist-Mangel IL1RN IL1RN 3-5
NULL
Isovalerianazidämie IVD IVD 5-6
CACNB4 CACNB4 34-35
CACNG4 CACNG4 NULL
- FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR FGFR1, PROKR2, PROK2, KISS1R, NELF, GNRH1, GNRHR 3-4
- KISS1R KISS1R 2-4
- TACR3 TACR3 2-4
NGS 4-8
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 1 KAL1/ANOS1 KAL1/ANOS1 2-4
Typ 2 FGFR1 FGFR1 2-4
Typ 3 PROKR2 PROKR2 2-4
Typ 5 CHD7 CHD7 2-4
Typ 5 CHD7 CHD7 2-4
Typ 6 FGF8 FGF8 2-4
TNNI3 TNNI3 2-4
dilatativ / hypertrophe NEXN NEXN 2-4
dilatative ACTN2 ACTN2 NULL
dilatative TNNT2 TNNT2 2-4
dilatative MYH7 MYH7 2-4
dilatative oder hypertrophe MYBPC3 MYBPC3 2-4
familiäre isolierte arrhythmogene ventrikuläre DSG2 DSG2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
familiäre isolierte arrhythmogene ventrikuläre PKP2 PKP2 2-4
hypertrophe TPM1 TPM1 NULL
hypertrophe RBM20 RBM20 2-4
LDB3 LDB3 NULL
MYH6 MYH6 2-4
MYOM1 MYOM1 2-4
PLN PLN NULL
SLC25A3 SLC25A3 3-4
NGS ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PLN, PRKAG2, SLC25A4, SOS1, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ACTC1, ACTN2, ALPK3, ANKRD1, CALR3, CAV3, CSRP3, FHL1, GLA, JPH2, LAMP2, LDB3, MYBPC3, MYH6, MYH7, M 4-8
LMNA LMNA 2-4
TTN TTN NULL
NHS NHS 2-4
Typ 17 CRYBB1 CRYBB1 2-4
Typ 2 CRYGC CRYGC 2-4
Typ 3 CRYBB2 CRYBB2 2-4
Typ 31 CHMP4B CHMP4B 2-4
Typ 4 CRYGD CRYGD 2-4
Typ 9 CRYAA CRYAA 2-4
Kaudale Regressions-Sequenz VANGL1 VANGL1 5-6
Kearns-Sayre-Syndrom MTTL2 MTTL2 3-4
NGS ACADM, ACADVL, HADHA, HADHB, HMGCL, HMGCS2 ACADM,ACADVL,HADHA,HADHB,HMGCL,HMGCS2 4-8
3-Hydroxyisobutyrat-Dehydrogenase-Mangel HIBADH HIBADH 2-4
NGS ACAT1, GYS2, HIBADH, HMGCL, HSD17B10, OXCT1, SLC16A1 ACAT1,GYS2,HIBADH,HMGCL,HSD17B10,OXCT1,SLC16A1 2-4
Ketothiolase-Mangel ACAT1 ACAT1 2-4
MGP MGP 4-6
ACAN, FGFR3, GH1, GHR, GHRHR, GHSR, IGF1, IGF1R, IGFALS, IHH, NPR2, SHOX, STAT5B ACAN,FGFR3,GH1,GHR,GHRHR,GHSR,IGF1,IGF1R,IGFALS,IHH,NPR2,SHOX,STAT5B 4-6
ACAN, COL10A1, COL2A1, COMP, FGFR3, IHH, NPR2, PTH1R, PTHLH, ROR2, SHOX ACAN,COL10A1,COL2A1,COMP,FGFR3,IHH,NPR2,PTH1R,PTHLH,ROR2,SHOX 4-6
BRAF, CREBBP, CUL7, DHCR7, HRAS, NIPBL, PTPN11 BRAF,CREBBP,CUL7,DHCR7,HRAS,NIPBL,PTPN11 4-6
diastrophischer SLC26A2 SLC26A2 2-4
Typ 1 GDF6 GDF6 8-20
Typ 3 GDF3 GDF3 8-20
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, TET2, TP53, U2AF1 ASXL1, BCOR, BCORL1, CBL, DNMT3A, GNAS, IDH1, IDH2, JAK2, KRAS, NRAS, PPM1D, PTPN11, SF3B1, SRSF2, T 2
NGS RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, PALB2, MPL, SBDS... RCA2 (FANCD1), BRIP1 (FANCJ), FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, 4-8
POLE1 POLE1 4-6
hereditäres nicht polypöses PMS2 PMS2 4-6
hereditäres nicht polypöses NULL
Immunhistochemie (MLH1, MSH2, MSH6, PMS2) 3-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
CARS2 CARS2
kombinierter Faktor 5 und 8-Mangel LMAN1 LMAN1 4-6
verschiedene Gene für CFEOM verschiedene Gene für CFEOM 4-8
kongenitalse malabsorptive Diarrhoe NEUROG3 NEUROG3 4-8
1-2
LARGE assoziierte Erkrankungen LARGE LARGE 5-6
amyotrophe FUS FUS 8
amyotrophe CHCHD10 CHCHD10 2-4
amyotrophe KIF5A KIF5A 3-4
amyotrophe SOD1 SOD1 3-4
amyotrophe 14 VCP VCP 2-6
amytrophe ALS2, ANG, ATXN2, DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... ALS2, ANG, ATXN2,DAO, FIG4, FUS, KIF5A, OPTN, PFN1, PON1, ... 4-8
Primäre PLS PLS NULL
Typ 2 ALS2 ALS2 1-9 / 100 000
- DTHD1 DTHD1 3-4
Typ 1 GUCY2D GUCY2D 4-5
Typ 10 CEP290 CEP290 3-5
Typ 11 IMPDH1 IMPDH1 3-4
Typ 12 RD3 RD3 3-4
Typ 13 RDH12 RDH12 3-4
Typ 14 LRAT LRAT 3-4
Typ 15 TULP1 TULP1 3-4
Typ 16 KCNJ13 KCNJ13 3-4
Typ 2 RPE65 RPE65 3-4
Typ 3 SPATA7 SPATA7 3-4
Typ 4 AIPL1 AIPL1 4-6
Typ 5 LCA5 LCA5 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 6 RPGRIP1 RPGRIP1 3-4
Typ 7 CRX CRX 3-4
Typ 7 GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) GUCY2D; RDH12; RPGRIP1; CEP290 (nur Intron 26) 3-4
Typ 8 CRB1 CRB1 4-5
Typ 8 AIPL1, CRB1, CRX, LCA5, RPE65 AIPL1, CRB1, CRX, LCA5, RPE65 2-4
Typ 9 NMNAT1 NMNAT1 3-4
Lebersche Hereditäre Optikusneuropathie MT-ND1, MT-ND4, MT-ND6 MT-ND1, MT-ND4, MT-ND6 2-4
Leigh-Syndrom SURF1 SURF1 2-4
COL4A6 COL4A6 2-4
EL EL
GABRB3 GABRB3 2-4
Leukenzephalopathie 4-8
megalenzephalen, mit subkortikalen Zysten HEPACAM HEPACAM 8-20
megalenzephalen, mit subkortikalen Zysten MLC1 MLC1 8-20
mit axonalen Sphäroiden und pigmentierter Glia CSF1R CSF1R 8-20
mit Hirnstamm- und Rückenmark DARS2 DARS2 8-12
zystische, ohne Megalenzephalie RNASET2 RNASET2 8-20
CEBPA, cKIT CEBPA, cKIT NULL
GATA2 GATA2 NULL
qualitativ PML-RARA PML-RARA 1
quantitativ PML-RARA PML-RARA 1-2
NGS ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 ASXL1, CALR, CBL, CSF3R, ETNK1, EZH2, JAK2, KRAS, MPL, NRAS, RUNX1, SETBP1, SRSF2, TET2, U2AF1 2
- DNMT3A DNMT3A 2
- NRAS NRAS 2
NGS JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 JAK2, JAK1, CRLF2, KRAS, NRAS, PTPN11, IKZF1, ASXL1, ARID2, CHD2, TP53 2
- TP53 TP53 2
LH-Resistenz LHCGR LHCGR 2-4
Typ 1 LIS1/PAFAH1B1 LIS1/PAFAH1B1 4-5
Typ 2 RELN RELN 8-12
X-chromosomal DCX DCX 8-9
TUBA1A TUBA1A NULL
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR1 TGFBR1 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 2-4
Loeys-Dietz-Syndrom TGFBR2 TGFBR2 3-5
LRP5 LRP5 2-3
- IGH/BCL2 IGH/BCL2 2
NGS BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 BCL2, CREBBP, EP300, EZH2, KMT2D (MLL2), MEF2B, TP53 2
NGS DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 DNMT3A, IDH2, RHOA, STAT3, TET2, TP53 2
lysinurische Proteinintoleranz SLC7A7 SLC7A7 2-4
- CDH1 CDH1 4-6
Majeed-Syndrom LPIN2 LPIN2 4-6
NULL
Makuladystrophie, vitelliforme BEST1 BEST1 3-4
PLCB1 PLCB1 NULL
Marfan-Syndrom FBN1 FBN1 2-4
Marfan-Syndrom FBN1 FBN1 2-4
NGS FBN1, TGFBR1, TGFBR2 FBN1,TGFBR1,TGFBR2 4-6
NGS ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 ASXL1, CBL, ETNK1, EZH2, IDH1, IDH2, JAK2, KIT, KRAS, NRAS, RUNX1, SRSF2, TET2, U2AF1 2
GNAS GNAS 4-6
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
Medium-chain-Acyl-CoA-Dehydrogenase-Mangel ACADM ACADM 2-4
AKT3 AKT3 NULL
4 CDT1 CDT1 NULL
Meier-Gorlin-Syndrom 1 ORC1 ORC1 7-8
MELAS-Syndrom MT-TL1 MT-TL1 2-4
FLNA FLNA 4-6
FLNA FLNA 6-8
ATRX ATRX NULL
AUTS2 AUTS2 NULL
4-8
TAOK2 TAOK2
TRIO TRIO NULL
MERRF-Syndrom MTTK MTTK 2-4
metachromatische Leukodystrophie ARSA ARSA 4-6
Typ Schmid COL10A1 COL10A1 3-4
HIBCH HIBCH 2-4
Methionin-Adenosyltransferase-Mangel MAT1A MAT1A 6-8
Methylmalonat-Semialdehyd-Dehydrogenase-Mangel ALDH6A1 ALDH6A1 6-7
cbl C MMACHC MMACHC 2-4
cbl C MMACHC MMACHC 2-4
cbl D MMADHC MMADHC 2-4
Methylmalonyl-CoA-Mutase-Mangel MMUT MMUT 6-8
Sequenzanalyse MMUT MMUT MMUT 2-4
familiäre hemiplegische ATP1A2, CACNA1A, NOTCH3, SCN1A ATP1A2, CACNA1A, NOTCH3, SCN1A 4-8
familiäre hemiplegische 1 CACNA1A CACNA1A 4-6
familiäre hemiplegische 2 ATP1A2 ATP1A2 8-10
familiäre hemiplegische 3 SCN1A SCN1A 4-5
Mikrolissenzephalie NDE1 NDE1 NULL
SLC25A22 SLC25A22 2-4
LIG4 LIG4 4-6
4-8
- CEP63 CEP63 3-5
- IER3IP1 IER3IP1 3-5
- KIF11 KIF11 3-5
- MYO16 MYO16 3-5
- PCNT PCNT 3-5
- RBBP8 RBBP8 4-6
- RTTN RTTN 3-5
- SLC25A19 SLC25A19 3-5
- TRAPPC9 TRAPPC9 3-5
- TUBB2B TUBB2B 3-5
MCPH1 MCPH1 MCPH1 3-5
MCPH2 WDR62 WDR62 3-5
MCPH3 CDK5RAP2 CDK5RAP2 3-5
MCPH4 CASC5 CASC5 3-5
MCPH4, MCPH9 CEP152 CEP152 3-5
MCPH5 ASPM ASPM 3-5
MCPH6 CENPJ CENPJ 3-5
MCPH8 CEP135 CEP135 5-7
Seckel syndrome ATR ATR 3-5
- PLK4 PLK4 2-4
LMNB1 LMNB1
SPATA5 SPATA5 NULL
QARS QARS NULL
mitochondrialer trifunktionaler Protein-Mangel HADHB HADHB 4-8
FBXL4 FBXL4 NULL
MNGIE-Syndrom TYMP, POLG, MGME1, RRM2B TYMP, POLG, MGME1, RRM2B 4-6
MNGIE-Syndrom TYMP TYMP 2-4
4-8
Typ A MOCS1 MOCS1 9-10
Typ B MOCS2 MOCS2 9-10
Typ C GPHN GPHN 4-8
KRT86 KRT86 4-8
Morbus Darier ATP2A2 ATP2A2 4-6
Morbus Krabbe GALC GALC 6-10
NGS ACVRL1, ENG, SMAD4, GDF2 ACVRL1, ENG, SMAD4, GDF2 4-6
Typ 1 ENG ENG 4-6
Typ 1,2 ENG, ACVRL1 ENG, ACVRL1 2-3
Typ 2 ACVRL1 ACVRL1 4-6
Typ 5 GDF2 GDF2 4-6
Morbus Wilson ATP7B ATP7B 2-4
Morbus Wilson ATP7B ATP7B 2-4
NGS ATP7B ATP7B 2-4
NULL
Mowat-Wilson-Syndrom ZEB2/ZFHX1B ZEB2/ZFHX1B 5-6
Muenke-Syndrom FGFR3 FGFR3 1-2
multi-drug-Resistenz ABCB1/MDR1 ABCB1/MDR1 2-3
PLAGL1, GRB10, MEST, H19, KCNQ1OT1, DLK1, MEG3, RTL1, SNRPN, PEG3, GNAS PLAGL1,GRB10,MEST,H19,KCNQ1OT1,DLK1,MEG3,RTL1,SNRPN,PEG3,GNAS 2-4
NGS BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 BRAF, DIS3, FAM46C, KRAS, NRAS, TP53 2
multiples Pterygium-Syndrom CHRNG CHRNG 4-6
Muskel-Augen-Gehirn-Krankheit POMGNT1 POMGNT1 5-6
RAPSN RAPSN NULL
kongenitales CHRND CHRND 5-6
MUSK MUSK NULL
NGS ASXL1, CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 ASXL1,CBL, EZH2, ETNK1, IDH2, JAK2, KIT, SETBP1, SF3B1, TET2 2
- AMH AMH 2-3
- AMHR2 AMHR2 2-3
- AMH, AMHR2 AMH,AMHR2 3-4
NGS PDGFRB, NOTCH3 PDGFRB, NOTCH3 4-8
rekurrente, genetisch bedingte LPIN1 LPIN1 2-4
juvenile CACNA1A CACNA1A 34-35
juvenile CACNA2D2 CACNA2D2 8-12
CLCN2 CLCN2 NULL
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP 4-6
4-6
4-6
SGCA, SGCB, SGCD, SGCG und FKRP SGCA, SGCB, SGCD, SGCG und FKRP
SEPN1 SEPN1 3-4
distale ACTA1, ANO5, CAV3, CRYAB, DES, DYSF, FHL1, FLNC, GNE, KLHL9, LDB3, MATR3, MYH14, MYH7, MYOT, NEB, RYR1, TCAP, TIA1, TPM3, VCP ACTA1,ANO5,CAV3,CRYAB,DES,DYSF,FHL1,FLNC,GNE,KLHL9,LDB3,MATR3,MYH14,MYH7,MYOT,NEB,RYR1,TCAP,TIA1,TPM 4-8
metabolische AGL, CPT2, ETFA, ETFB, ETFDH, GAA, GBE1, LPIN1, PFKM, PYGM, RRM2B, SLC22A5 und weitere AGL,CPT2,ETFA,ETFB,ETFDH,GAA,GBE1,LPIN1,PFKM,PYGM,RRM2B,SLC22A5 und weitere 4-8
NGS verschiedene Gene für MYOP verschiedene Gene für MYOP 4-8
Becker, Thomsen CLCN1 CLCN1 2-4
Becker, Thomsen CLCN1 CLCN1 2-4
X-linked MTM1 MTM1 3-4
N-Acetylglutamat-Synthetase-Mangel NAGS NAGS 2-4
N-Acetyltransferase 2-Mangel NAT2 NAT2 2-3
NACC1 NACC1 NULL
ANKLE2 ANKLE2 NULL
DCHS2 DCHS2 NULL
DNAJB9 DNAJB9 NULL
NRK NRK NULL
PIP5K1A PIP5K1A NULL
PLEKHG4 PLEKHG4 NULL
PRDM9 PRDM9 NULL
SRSF5 SRSF5 NULL
TOE1 TOE1 NULL
DNAJC3 DNAJC3 NULL
NGS diverse Gene diverse Gene 4-8
autosomal dominant 2 PDE6B PDE6B 4-6
Autosomal dominant, Typ 1 RHO RHO 4-6
Autosomal dominant, Typ 3 GNAT1 GNAT1 4-6
autosomal-rezessiv, Typ 1B GRM6 GRM6 4-5
autosomal-rezessiv, Typ 1C TRPM1 TRPM1 4-5
autosomal-rezessiv, Typ 1E GPR179 GPR179 4-5
autosomal-rezessiv, Typ 1F LRIT3 LRIT3 3-4
autosomal-rezessiv, Typ 2B CABP4 CABP4 4-5
Typ 1D SLC24A1 SLC24A1 3-4
X-chromosomal, Typ 1A NYX NYX 3-4
X-chromosomal, Typ 2A CACNA1F CACNA1F 4-5
Nagel-Patella-Syndrom LMX1B LMX1B 3-4
Nagel-Patella-Syndrom LMX1B LMX1B 2-3
NULL
Natrium-Diarrhoe, kongenitale SPINT2 SPINT2 NULL
- KLHL41 KLHL41 4-6
Typ Amish TNNT1 TNNT1 4-5
NPHP1 NPHP1 NPHP1 2-5
NPHP1 NPHP1 NPHP1 2-3
Netherton-Syndrom SPINK5 SPINK5 4-5
APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR APOA1, APOA2, APP, B2M, CST3, FGA, GSN, ITM2B, LYZ, PRNP, TTR 4-6
4-8
Typ 2 4-8
GNAO1 GNAO1
Typ Fiskerstrand ABHD12 ABHD12 3-4
kongenital schwere 3 HAX1 HAX1 4-6
kongenital schwere 6 JAGN1 JAGN1 4-8
kongenitale schwere 1 ELANE/ELA2 ELANE/ELA2 2-4
somatische Mutationen CSF3R, TP53 CSF3R, TP53 2
X-chromosomal WAS WAS 4-8
NGS CSF3R, SETBP1, ASXL1 CSF3R, SETBP1, ASXL1 2
NFE2L3 NFE2L3 NULL
NULL
1-2
nicht-ketotische Hyperglycinämie GCSH GCSH 3-4
NGS 4-8
pappilär MET MET 2-4
NGS BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL BAP1, FH, FLCN, MET, MITF, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHL 4-6 Wochen
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
Nijmegen-Chromosomenbruch-Syndrom NBN NBN 4-5
NBN NBN 2-4 Wochen
NGS NF1, NF2, CBL, NRAS, KRAS, PTPN11 NF1, NF2, CBL, NRAS, KRAS, PTPN11 4-6
NDP NDP 2-4
verschiedene Gene für NYS verschiedene Gene für NYS 4-8
Typ 1 FRMD7 FRMD7 2-4
Typ 1 FRMD7 FRMD7 2-4
Typ 6 GPR143 GPR143 2-4
LRIG2 LRIG2 NULL
Okihiro-Syndrom SALL4 SALL4 4-6
Ornithintranscarbamylase-Mangel OTC OTC 5-8
Ornithintranscarbamylase-Mangel OTC OTC 3-4
NGS COL1A1, COL1A2, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, .. COL1A1,COL1A2,CRTAP,FKBP10,LEPRE1,PPIB,SERPINF1,.. 4-8
Typ 12 SP7 SP7 4-8
NGS LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 LMNA, MAFB, MMP14, MMP2, NOTCH2, TNFRSF11A, TREM2, TYROBP, ZMPSTE24 4-6
Typ 2, 4 CLCN7 CLCN7 5-6
Typ 1 TCIRG1 TCIRG1 5-6
Typ 2 TNFSF11 TNFSF11 5-6
Typ 5 OSTM1 OSTM1 5-6
Typ 7 TNFRSF11A TNFRSF11A 5-6
X-chromosomal PLS3 PLS3 4-8
LRP5 LRP5 3-4
FLNA FLNA NULL
2 KRT17 KRT17 4-8
NGS KRT16, KRT17, KRT6A, KRT6B, KRT6C KRT16, KRT17, KRT6A, KRT6B, KRT6C 4-8
NGS BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 BRCA1, BRCA2, CDKN2A, MEN1, PALB2, PALLD, PRSS1, TP53, SPINK1, STK11 4-8
- CDKN2A CDKN2A 3-4
Pankreatische Colipase-Mangel PNLIP PNLIP 2-4
PRSS1, SPINK1, CTRC PRSS1, SPINK1, CTRC 2-4
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär CFTR CFTR 1-3
Pankreatitis, hereditär PRSS1 PRSS1 3-4
Pankreatitis, hereditär SPINK1 SPINK1 3-4
SCN4A SCN4A 3-5
PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 PARK7 ATP13A2 PINK1 UCHL1 SNCA PARK2 CAV1/2 LRRK2 GCH1 2-3
17 VPS35 VPS35 4-8
23 VPS13C VPS13C 4-8
frühkindlich hypotonisch SLC18A2 SLC18A2 4-8
Parkinson-Krankheit LRRK2 LRRK2 4-8
Parkinson-Krankheit diverse diverse 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit PINK1 PINK1 4-8
Parkinson-Krankheit 1,4 SNCA SNCA 4-8
Typ 2 PRKN PRKN 4-8
paroxysmale nächtliche Hämoglobinurie PIGA PIGA 2-4
paroxysmale nächtliche Hämoglobinurie PIGA, PIGT PIGA,PIGT 2-4
partielle Chromosom Y-Deletion, AZF-Faktor USP9Y USP9Y 2-4
Parvovirus B19 1-2
Peeling-Skin-Syndrom TGM5 TGM5 5-7
PLP1 PLP1 2-3
PLP1 PLP1 2-3
Pelizaeus-Merzbacher-ähnliche Krankheit AIMP1 AIMP1 5-7
Pelizaeus-Merzbacher-ähnliche Krankheit GJC2 GJC2 4-5
Pelizaeus-Merzbacher-ähnliche Krankheit HSPD1 HSPD1 4-5
Pendred-Syndrom FOXI1, KCNJ10, SLC26A4 FOXI1, KCNJ10, SLC26A4 15-16
CLPP; HARS2, HSD27B4, LARS2 CLPP; HARS2, HSD27B4, LARS2 4-8
Autosomal-rezessiv HARS2 HARS2 2-4
Autosomal-rezessiv HSD17B4 HSD17B4 3-4
Typ 3 CLPP CLPP 3-4
Typ 4 LARS2 LARS2 3-4
ATOH7 ATOH7 2-4
- PAX6 PAX6 2-4
- PITX2 PITX2 2-4
B3GLCT B3GLCT 2-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 3-4
- STK11 STK11 4-8
- FGFR1 FGFR1 1-2
- FGFR1 FGFR1 3-4
- FGFR2 FGFR2 1-2
- FGFR2 FGFR2 3-4
- KIT KIT 3
Piebaldismus SNAI2 SNAI2 3-4
Piebaldismus SNAI2 SNAI2 3-4
Pierson-Syndrom LAMB2 LAMB2 2-4
RUNX1 RUNX1
RUNX1, GATA2, TERC, TERT, CEBPA RUNX1,GATA2,TERC,TERT,CEBPA 2-4 Wochen
IQCE IQCE
AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 AIRE, CTLA4, FOXP3, IL2RA, ITCH, JAK1, LRBA, STAT1, STAT3, STAT5B, TNFAIP3 NULL
autoimmun, Typ 1 AIRE AIRE 2 - 4
autoimmun, Typ 1 2 - 4
STRADA STRADA NULL
POLD1 POLD1
- SMAD4 SMAD4 4-8
- SMAD4 SMAD4 4-8
- ALG8 ALG8 3-4
- GANAB GANAB 3-4
- PRKCSH PRKCSH 3-4
- SEC63 SEC63 3-4
Typ 2C TSEN34 TSEN34 NULL
Porenzephalie 1 COL4A1 COL4A1 6-8
Porenzephalie 2 COL4A2 COL4A2 4-8
Porphyria variegata PPOX PPOX 8-20
akute intermittierende HMBS HMBS 8-20
SNRPN SNRPN 2-4
PDE11A PDE11A 2-4
4-8
Typ 1 ATP8B1 ATP8B1 2-4
Typ 2 ABCB11 ABCB11 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 3 ABCB4 ABCB4 2-4
Typ 4 TJP2 TJP2 2-4
NGS AIP, DICER, MEN1, SDHB AIP, DICER, MEN1, SDHB 4-6
Protein-C-Rezeptor-Mangel PROCR PROCR 3-4
NGS AKT1, PIK3CA, PTEN AKT1, PIK3CA, PTEN 4-6
AKT1 AKT1 3-4
Pseudoachondroplasie COMP COMP 2-4
GNAS GNAS 2-4
Pseudoxanthoma elasticum ABCC6 ABCC6 NULL
Pseudoxanthoma elasticum ABCC6 ABCC6 2-4
Pyruvat-Carboxylase-Mangel PC PC 2-4
PHYH PHYH 4-6
NLRP7/NALP7, KHDC3L, MEI1, C11orf80 NLRP7/NALP7, KHDC3L, MEI1, C11orf80
NULL
NGS 4-6
restriktive Dermopathie ZMPSTE24 ZMPSTE24 6-8
SMARCB1 SMARCB1 2-3 Wochen
Roberts-Syndrom ESCO2 ESCO2 2-4
autosomal-dominant DVL1 DVL1 4-6
autosomal-dominant WNT5A WNT5A 2-4
autosomal-rezessiv ROR2 ROR2 2-4
autosomal-rezessiv ROR2 ROR2 2-3
Schilddrüsen-Dyshormonogenese TPO TPO 2-4
DUOX2 DUOX2 2-4
NGS DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRH, TSHB, TSHR, TTF1, TTF2, UBR1 DUOX2, DUOXA2, GLIS3, GNAS, IGSF1, IYD, LHX3, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SLC16A2 4-8
TPO, PAX8, FOXE1, NKX2-1, TSHR TPO, PAX8, FOXE1, NKX2-1, TSHR 2-4
NULL
sehr langkettige-Acyl-CoA-Dehydrogenase-Mangel ACADVL ACADVL 2-4
ASXL2 ASXL2 NULL
SHOX-Defizienz SHOX SHOX 2-4
SHOX-Defizienz SHOX SHOX 2-4
NEU1 NEU1 NULL
Sialinsäure-Speicherkrankheit SLC17A5 SLC17A5 4-6
Methylierungsanalyse H19-DMR und KvDMR1 H19, KCNQ1OT1 H19,KCNQ1OT1 2-4
MLPA Analyse UPD(7)mat GRB10, MEST GRB10,MEST 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 2-4
ALDH3A2/FALDH ALDH3A2/FALDH 3-5
NGS AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPGD, IKBKG, KL, LEMD3, LRP4, LRP5, LRRK1, MAP2K1, MTAP, OSTM1, PLEKHM1, POLR3B, PTDSS1, PTH1R, SFRP4, SLC29A3, SLCO2A1, SNX10, SOST, TBXAS1, TCIRG1, ..... AMER1, ANKH, CA2, CLCN7, COL1A1, CSF1R, CTSK, DHCR24, DLX3, FAM20C, FERMT3, FGF23, GALNT3, GJA1, HPG 4-6
NGS ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, IFIH1, IFITM5, LRP5, MBTPS2, NBAS, NOTCH2, P3H1, P4HB, PLOD2, PLS3, POLR3A, PPIB, PYCR1, SEC24D, SERPINF1, SERPINH1, SGMS2, SP7, SPARC, TENT5A, ........ ALPL, ANO5, ATP6V0A2, B3GALT6, B4GALT7, BMP1, COL1A1, COL1A2, CREB3L1, CRTAP, DDX58, FKBP10, GORAB, 4-6
Typ Charlevoix-Saguenay SACS SACS 14-16
Typ 11 SPG11 SPG11 4-5
Typ 17 BSCL2 BSCL2 4-5
Typ 3 ATL1 ATL1 2-4
Typ 3 ATL1 ATL1 2-3
Typ 31 REEP1 REEP1 3-4
Typ 4 SPAST SPAST 2-4
Typ 4 SPAST SPAST 2-3
Typ 5 CYP7B1 CYP7B1 3-4
Typ 6 NIPA1 NIPA1 NULL
Typ 7 SPG7 SPG7 8-12
Typ 8 KIAA0196 KIAA0196 NULL
DDHD2 DDHD2 NULL
WASHC5 WASHC5 NULL
PNPLA6 PNPLA6 NULL
Typ 1 IGHMBP2 IGHMBP2 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 3-4
Typ 1, 2, 3, 4 SMN1 SMN1 10-14
Typ 3 SMN2 SMN2 2-3
Typ trada TRAPPC2 TRAPPC2 2-4
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 4-6
kongenitaler Typ COL2A1 COL2A1 2-3
MATN3 MATN3 NULL
Stargardt-ähnliche Makuladystrophie IMPG1 IMPG1 2-4
COL27A1 COL27A1 NULL
Sterilität, CBAVD CFTR CFTR 3-4
Sterilität, CBAVD CFTR CFTR 3-4
Steroid-5-alpha-Reduktase-2-Mangel SRD5A2 SRD5A2 2-4
COL11A1 COL11A1 2-4
NGS verschiedene Gene für STICK verschiedene Gene für STICK 4-8
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 4-6
Typ 1 COL2A1 COL2A1 2-3
Typ 2 COL11A1 COL11A1 4-6
Typ 2 COL11A1 COL11A1 2-4
Stuve-Wiedemann-Syndrom LIFR LIFR 6-8
Störungen der Geschlechtsentwicklung NR5A1 NR5A1 2-4
WNT9B WNT9B 2-4
Surfactant-Protein-Defizienz SFTPC SFTPC 3-4
Surfactant-Protein-Defizienz ABCA3 ABCA3 3-4
Surfactant-Protein-Defizienz ABCA3, SFTPC ABCA3, SFTPC 2-4
Surfactant-Protein-Defizienz SFTPB SFTPB 3-4
Surfactant-Protein-Defizienz SFTPB SFTPB 2-3
NGS ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC ABCA3, CSF2RA, CSF2RB, NKX2-1, SFTPB, SFTPC 6-8
NULL
proximaler GDF5 GDF5 3-4
proximaler NOG NOG 1-3
autoimmun-lymphoproliferatives Typ 2 CASP10 CASP10 2-4
MED13 MED13
NGS diverse Gene diverse Gene 4-8
NGS CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SLC29A3, STAT3, TRMT10A, WFS1 CISD2, DCAF17, DNAJC3, EIF2AK3, FOXP3, GATA4, GATA6, GLIS3, IER3IP1, MT-TL1, PAX6, RFX6, SLC19A2, SL 4-8
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
systemische juvenile rheumatoide Arthritis IL6 IL6 1-2
T-Zell-Rezeptor-gamma-Rearrangement TCRG TCRG 2-3
RBM10 RBM10 3-4
AR AR 2-4
HBA1, HBA2, HBB HBA1, HBA2, HBB 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Alpha HBA1, HBA2 HBA1, HBA2 2-4
Beta HBB HBB 2-4
Beta HBB HBB 2-4
HPFH HBG1, HBG2 HBG1, HBG2 3-4
SLC19A2 SLC19A2 2-4
Thrombotisch-thrombozytopenische Purpura ADAMTS13 ADAMTS13 2-4
MITF MITF 3-4
Transaldolase-Mangel TALDO1 TALDO1 6-8
Treacher-Collins-Syndrom POLR1C POLR1C 3-4
Treacher-Collins-Syndrom POLR1D POLR1D 3-4
Treacher-Collins-Syndrom TCOF1 TCOF1 6-8
Treacher-Collins-Syndrom TCOF1 TCOF1 2-3
MLPA TRPS1 TRPS1 2-4
Trimethylaminurie FMO3 FMO3 2-4
TSC1, TSC2 TSC1,TSC2 2-3
Typ 1 TSC1 TSC1 3-4
Typ 2 TSC2 TSC2 4-5
2-3
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Tumor-Prädispositionssyndrom BAP1 BAP1 2-4
Typ 1 FAH FAH 4-6
KCNB1 KCNB1 NULL
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
2-4
CSTB CSTB 3-4
Unverricht Lundborg Epilepsie CSTB CSTB 4-5
NGS divers divers 4-8
Typ 1B MYO7A MYO7A 2-4
Typ 1C USH1C USH1C 2-4
Typ 1D CDH23 CDH23 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1F PCDH15 PCDH15 2-4
Typ 1G USH1G USH1G 2-4
Typ 1J CIB2 CIB2 2-4
Typ 2 D DFNB31 DFNB31 2-4
Typ 2A USH2A USH2A 2-4
Typ 2A USH2A USH2A 2-4
Typ 2C GPR98/ADGRV1 GPR98/ADGRV1 2-4
Typ 3A USH3A USH3A 2-3
Typ 3B HARS HARS 2-4
Typ 48 CIB2 CIB2 3-4
Van-der-Woude-Syndrom IRF6 IRF6 4-6
Vitamin-E-abhängige Ataxie TTPA TTPA 5-6
GHRHR GHRHR 2-4
GH1 GH1 2-4
VCAN VCAN NULL
- WT1 WT1 3-4
B3GALNT2 B3GALNT2 NULL
ISPD ISPD NULL
4-8
POMT1 POMT1 NULL
POMT2 POMT2 3-4
TMEM5 TMEM5 NULL
WARS WARS NULL
Wiedemann-Steiner-Syndrom KMT2A/MLL1 KMT2A/MLL1 4-6
NULL
Williams Beuren Syndrom CLIP2, ELN, LIMK CLIP2, ELN, LIMK 3-4
Typ 2 CISD2 CISD2 2-4
WWP2 WWP2
4-8
X-chromosomales Hyper-IgM-Syndrom CD40LG, CD40, UNG, AICDA CD40LG, CD40, UNG, AICDA 5-6 Wochen
4-6
Typ 1 XDH XDH 2-4
primäre PTH1R PTH1R 4-6
diverse diverse 4-8
X-gekoppelt ORF15, RPGR ORF15, RPGR 4-8
zerebraler cavernöse Fehlbildungen KRIT1, CCM2, PDCD10 KRIT1, CCM2, PDCD10 4-8
PKD1, PKD2, DNAJB11, GANAB, ALG9 PKD1,PKD2,DNAJB11,GANAB,ALG9 12-18
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
4-8
NULL
NPHP1, NPHP3, NPHP4, IQCB1, CEP290, SDCCAG8 NPHP1, NPHP3,NPHP4, IQCB1,CEP290,SDCCAG8 4-8
NULL
NULL
NGS 4-8
Renal tubuläre Dysgenesie 12
8-12
SLC30A2 SLC30A2 4-6
ALG9 ALG9 2-4
Fumarazidurie (FH)      
CHD4 CHD4 NULL
GOLGA2 GOLGA2 NULL
PRIMA1 PRIMA1 NULL
- GLI3 GLI3 3-5
- GLI3 GLI3 2-3
ALAD ALAD 4-8
8-12
4-6
4-6
4-6
4-6
4-6
BCKDK BCKDK 2-4
SLC19A3 SLC19A3 2-4
NGS CACNA1C, CACNA2D1, CACNB2, HCN4, KCNE3, SCN3B, SCN5A, TRPM4 und weitere CACNA1C, CACNA2D1, CACNB2, HCN4, KCNE3, SCN3B, SCN5A, TRPM4 und weitere 4-8
Typ 1 SCN5A SCN5A 4-6
Typ 4 CACNB2 CACNB2 NULL
Typ 8 HCN4 HCN4 4-8
NGS MYC, ARID1A, CCND3, CREBBP, GNA13, ID3, TP53 MYC, ARID1A, CCND3, CREBBP, GNA13, ID3, TP53 2
Börjeson-Forssman-Lehmann-Syndrom PHF6 PHF6 2-4
HTRA1 HTRA1 NULL
idiopathische UNC119 UNC119 2-4
NULL
NGS AIRE, CARD9, CLEC7A, IL17F, IL17RA, IL17RC, PTPN22, STAT1, TLR3, TRAF3IP2 AIRE, CARD9, CLEC7A, IL17F, IL17RA, IL17RC, PTPN22, STAT1, TLR3, TRAF3IP2 4-6
Typ 1 FBLN4/EFEMP2 FBLN4/EFEMP2 8-12
Typ 1 FBLN5 FBLN5 4-6
DiGeorge-Syndrom TBX1 TBX1 4-5
Doynsche Honigwabendystrophi EFEMP1 EFEMP1 3-4
ADAR ADAR 2-4
Dyskeratosis congenita DKC1 DKC1 4-6
NGS CTC1, DKC1, RTEL1, TERC, TERT, TINF2, ACD, NHP2 CTC1, DKC1, RTEL1, TERC, TERT, TINF2, ACD, NHP2 4-8
NGS B3GALT6, B3GAT3, BPNT2, CANT1, CHST3, CSGALNACT1, EXOC6B, FAM20B, FKBP14, FLNB, GZF1, KIF22, PLOD1, SLC10A7, SLC26A2, XYLT1 B3GALT6, B3GAT3, BPNT2, CANT1, CHST3, CSGALNACT1, EXOC6B, FAM20B, FKBP14, FLNB, GZF1, KIF22, PLOD1, 4-6
VLDLR VLDLR NULL
epidermolytische palmoplantare Keratose KRT9 KRT9 4-8
PCDH19 PCDH19 NULL
6-10
- FANCD1/BRCA2 FANCD1/BRCA2 4-8
FH FH 2-4
Galaktokinase-Mangel GALK1 GALK1 2-4
6-10
MCM4 MCM4 2-4
FGD Typ 1 MC2R MC2R 2-4
FGD Typ 2 MRAP MRAP 2-4
Glutaryl-CoA-Dehydrogenase-Mangel GCDH GCDH 8-12
GYG1 GYG1 2-4
RFT1 RFT1 3-6
kongenitaler PMM2, MPI, ALG6, ALG3, DPM1, MPDU1, ALG12, ALG8, ALG2, DPAGT1, ALG1, ALG9, DOLK, RFT1, DPM3, ALG11, SRD5A3, DDOST, ALG13, PGM1, DPM2, STT3A, STT3B, SSR4, ATP6V0A2, MAGT1, TUSC3, DHDDS, GMPPA, PGM3, NUS1 PMM2, MPI, ALG6, ALG3, DPM1, MPDU1, ALG12, ALG8, ALG2, DPAGT1, ALG1, ALG9, DOLK, RFT1, DPM3, ALG11, 4-8
kongenitaler B4GALT1, CCDC115, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MAN1B1, MGAT2, MOGS, SLC35A1, SLC35A2, SLC35C1, SLC39A8, ST3GAL3, TMEM165, TMEM199 B4GALT1, CCDC115, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MAN1B1, MGAT2, MOGS, SLC35A1, SLC35A2, S 4-8
kongenitaler MGAT2 MGAT2 4-8
kongenitaler ALG1, ALG11, ALG12, ALG2, ALG3, ALG6, ALG8, ALG9, DOLK, DPAGT1, DPM1, MAGT1, MPDU1, MPI, PGM1, PGM3, PMM2, RFT1, SRD5A3, TUSC3, B4GALT1, COG1, COG2, COG4, COG5, COG6, COG7, COG8, MGAT2, MOGS, SLC35A1, SLC35A2, SLC35C1, TMEM165 ALG1, ALG11, ALG12, ALG2, ALG3, ALG6, ALG8, ALG9, DOLK, DPAGT1, DPM1, MAGT1, MPDU1, MPI, PGM1, PGM3, 4-8
kongenitaler Typ 1T PGM1 PGM1 2-4
kongenitaler, Typ 1 A PMM2 PMM2 4-8
kongenitaler, Typ 1B MPI MPI 2-4
kongenitaler, Typ 2 ALG9 ALG9 2-4
GRACILE-Syndrom BCS1L BCS1L 2-4
Gricelli-Syndrom verschiedene Gene für GS verschiedene Gene für GS 6-10
Typ 1 MYO5A MYO5A 6-10
Typ 2 RAB27A RAB27A 6-10
Typ 3 MLPH MLPH 4-8
ADAMTS3, CCBE1, CELSR1, EPHB4, FAT4, FLT4, FOXC2, GJC2, KIF11, PIEZO1, PTPN14, SOX18, VEGFC ADAMTS3, CCBE1, CELSR1, EPHB4, FAT4, FLT4, FOXC2, GJC2, KIF11, PIEZO1, PTPN14, SOX18, VEGFC 4-6 Wochen
Holocarboxylase-Synthetase-Mangel HLCS HLCS 4-5
- CETP CETP 2-4
NGS 4-6
PGAP3 PGAP3 NULL
NALCN NALCN NULL
juvenile Makuladegeneration CDH3 CDH3 4-5
Immundefizienz 47 ATP6AP1 ATP6AP1 4-8
infantile Hyperkalziurie CYP24A1 CYP24A1 2-4
ANKS4B ANKS4B 2-4
KMT2C KMT2C NULL
EHMT1 EHMT1 NULL
RNU4ATAC RNU4ATAC 6-8
letale Form FAM20C FAM20C 4-8
ROGDI ROGDI
MSH6, EPCAM MSH6, EPCAM 4-6
NGS MLH1, MSH2, MSH6, PMS2, EPCAM MLH1, MSH2, MSH6, PMS2, EPCAM 4-8
Typ 1 MSH2 MSH2 4-6
Typ 1 / 2 MLH1, MSH2 MLH1, MSH2 4-6
Typ 2 MLH1 MLH1 4-6
Typ 4 PMS2 PMS2 4-6
Typ 5 MSH6 MSH6 4-6
Typ 7 MLH3 MLH3 4-6
Typ 8 EPCAM EPCAM 4-8
Typ 8 EPCAM EPCAM 3-4
Laktoseintoleranz LCT LCT 1-3
- SPRED1 SPRED1 3-4
- SPRED1 SPRED1 3-4
NGS 2
hämophagozytische PRF1, STX11, UNC13D PRF1,STX11, UNC13D 2-4
hämophagozytische, Typ 2 PRF1 PRF1 4-8
hämophagozytische, Typ 3 UNC13D UNC13D 4-8
hämophagozytische, Typ 4 STX11 STX11 4-8
hämophagozytische, Typ 5 STXBP2 STXBP2 4-8
Typ cblA MMAA MMAA 2-4
Typ 1 und 2 CYB5R3 CYB5R3 2-4
Typ 1 und 2 CYB5R3 CYB5R3 4-8
TSC2, PKD1 TSC2, PKD1 2-3
NGS AARS2, ABCB7, ACAD9, ACADM, ACADS, ACADVL, ACO2, ADCK1, ADCK2, ADCK5, AFG3L2, AGK, AIFM1, AK2, APTX, ATP5F1A, ATP5F1E, ATPAF1, ATPAF2, AUH, BCS1L, BOLA3, C12orf65, C19orf12, CARS2, CHCHD10, CHKB, CLPB, CLPP, COA3, COA5, COA8, COASY, COQ10A, COQ10B, COQ2, COQ4, COQ5, COQ6, COQ7, COQ8A, COQ8B, COQ9 AARS2,ABCB7,ACAD9,ACADM,ACADS,ACADVL,ACO2,ADCK1,ADCK2,ADCK5,AFG3L2,AGK,AIFM1,AK2,APTX,ATP5F1A,ATP5F1 4-6
SLC5A8 SLC5A8 NULL
SON SON NULL
STAG2 STAG2 NULL
NQO1 NQO1 2-3
NGS 4-8
kongenitale schwere 4 G6PC3 G6PC3 4-8
NGS ELANE, G6PC3, HAX1, JAGN1, WAS ELANE, G6PC3, HAX1, JAGN1, WAS 4-8
- PLOD2 PLOD2 3-4
- SEC24D SEC24D 4-8
Typ 10 SERPINH1 SERPINH1 2-4
Typ 11 FKBP10 FKBP10 3-4
Typ 13 BMP1 BMP1 3-4
Typ 14 TMEM38B TMEM38B 3-4
Typ 15 WNT1 WNT1 3-4
Typ 6 CREB3L1 CREB3L1 4-8
Typ 6 SERPINF1 SERPINF1 3-4
Typ 7 CRTAP CRTAP 3-5
Typ 8 LEPRE1/P3H1 LEPRE1/P3H1 3-4
Typ 9 PPIB PPIB 3-4
MIPEP MIPEP NULL
mitochondrial 3-4
FLNA FLNA 4-6
TWNK TWNK 2-4
PNMT PNMT NULL
ADGRG1 ADGRG1 NULL
Porphyria cutanea tarda FECH, UROS, UROD and CPOX FECH, UROS, UROD and CPOX 2-4
Protein-S-Mangel PROS1 PROS1 4-6
NGS 4-6
Renal tubuläre Azidose, distal/proximal CA2 CA2 2-4
MECP2 MECP2 3-4
atypisches CDKL5 CDKL5 3-4
atypisches CDKL5 CDKL5 2-3
atypisches FOXG1 FOXG1 3-4
atypisches FOXG1 FOXG1 4-5
atypisches NTNG1 NTNG1 3-4
atypisches NTNG1 NTNG1 3-4
klassisches MECP2 MECP2 3-4
NGS DICER1, HRAS, NF1, PTPN11, TP53 DICER1, HRAS, NF1, PTPN11, TP53 4-6
NGS APC, CDKN1B, DICER1, FOXE1, HABP2, MEN1, NKX2-1, PRKAR1A, RET, PTEN, TP53 APC, CDKN1B, DICER1, FOXE1, HABP2, MEN1, NKX2-1, PRKAR1A, RET, PTEN, TP53 4-8
PAX3 PAX3 3-4
FLNB FLNB 2-3
FLNB FLNB 3-4
FLNB FLNB 5-6
NGS CYP21A2, CYP17A1, CYP11B1, HSD3B2, POR, STAR CYP21A2, CYP17A1, CYP11B1, HSD3B2, POR, STAR 4-8
NGS CLPP, CYP11B1, CYP21A2, FSHR, HARS2, HNF1B, HSD17B4, LARS2, LHCGR, LHX1, NR5A1, POR, PSMC3IP, RSPO1, SOX3, SOX9, SRY, WNT4 CLPP, CYP11B1, CYP21A2, FSHR, HARS2, HNF1B, HSD17B4, LARS2, LHCGR, LHX1, NR5A1, POR, PSMC3IP, RSPO1, 4-8
MLPA-Analyse UPD(14)mat 2-4
- ANKRD26 ANKRD26 4-6
- GATA1 GATA1 4-6
NGS 4-6
- THPO THPO 4-6
NGS JAK2, MPL, THPO JAK2, MPL, THPO 4-6
PCGF2 PCGF2
Typ 1 ASS1 ASS1 4-6
Typ 2 SLC25A13 SLC25A13 4-6
Fundus albipunctatus1,2,3      
HMGCL HMGCL 4-6
Typ 3 CLDN16 CLDN16 2-4
Typ 5 CLDN19 CLDN19 2-4
Fundus albipunctatus RDH5 RDH5 4-6

zum Seitenanfang

¹ Alle Gene für diese Erkrankung werden zur Testung angeboten. Da in einzelnen Fällen spezifische Genotyp-, Phänotyp-Korrelationen bestehen, bitten wir ggf. um Rücksprache, um eine möglichst gezielte Analyse vornehmen zu können.
² Kopplungsanalyse durchführbar, sinnvoll vor allem bei elterlicher Blutsverwandtschaft und/oder Vorliegen von Proben mehrerer Familienmitglieder.
³ Stufenanalyse
* Fremdlaborleistungen. Alle weiteren dargestellten Untersuchungen erbringen wir am Standort Ingelheim.

Nach Anfangsbuchstaben