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Victorian Clinical Genetics Services (Murdoch Childrens Research Institute), VCGS

General information

Victorian Clinical Genetics Services, VCGS
Murdoch Childrens Research Institute
50 Flemington Rd
Melbourne
Victoria
Australia - 3052
http://www.vcgs.org.au/pathology/
Organization ID: 500104

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 8629

Gene

GeneSubmissionsLast Updated
AAAS3Nov 19, 2024
AAGAB2Jul 18, 2024
AARS11Nov 19, 2024
AARS25Jul 18, 2024
ABAT2Nov 19, 2024
ABCA11Nov 19, 2024
ABCA123Jul 18, 2024
ABCA35Jul 18, 2024
ABCA440Nov 19, 2024
ABCB111Dec 21, 2022
ABCB414Nov 19, 2024
ABCB61Nov 19, 2024
ABCC69Nov 19, 2024
ABCC86Nov 19, 2024
ABCC99Nov 19, 2024
ABCD15Nov 19, 2024
ABCG51Jul 18, 2024
ABCG81Jul 18, 2024
ABHD14A-ACY11Nov 19, 2024
ABL11Jul 18, 2024
ACAD97Nov 19, 2024
ACADM6Nov 19, 2024
ACADS2Dec 21, 2022
ACADVL6Jul 18, 2024
ACAT11Dec 21, 2022
ACO23Nov 19, 2024
ACSL42Jul 18, 2024
ACSM31Jul 18, 2024
ACTA12Nov 19, 2024
ACTA28Nov 19, 2024
ACTA2-AS13Nov 19, 2024
ACTB11Nov 19, 2024
ACTC13Nov 19, 2024
ACTG13Nov 19, 2024
ACTG24Nov 19, 2024
ACTL6B4Nov 19, 2024
ACTN13Nov 19, 2024
ACTN27Nov 19, 2024
ACTN44Nov 19, 2024
ACVRL110Nov 19, 2024
ACY11Nov 19, 2024
ADA1Jul 18, 2024
ADA24Nov 19, 2024
ADAMTS101Jul 18, 2024
ADAMTS134Nov 19, 2024
ADAMTS21Dec 21, 2022
ADAMTSL22Dec 21, 2022
ADAMTSL44Nov 19, 2024
ADAMTSL4-AS22Nov 19, 2024
ADAR3Nov 19, 2024
ADAT31Nov 19, 2024
ADCY53Nov 19, 2024
ADGRG12Dec 21, 2022
ADGRG61Jul 18, 2024
ADGRL11Jul 18, 2024
ADGRL1-AS11Jul 18, 2024
ADGRV17Nov 19, 2024
ADIPOR11Nov 19, 2024
ADNP12Nov 19, 2024
ADSL2Jul 18, 2024
ADSS11Nov 19, 2024
AFF23Nov 19, 2024
AFF43Nov 19, 2024
AFG2A4Jul 18, 2024
AFG2B1Jul 18, 2024
AFG3L23Nov 19, 2024
AGK3Dec 21, 2022
AGL5Nov 19, 2024
AGO13Nov 19, 2024
AGPAT22Dec 21, 2022
AGRN1Jul 18, 2024
AGXT7Nov 19, 2024
AHDC17Nov 19, 2024
AHI16Jul 18, 2024
AIFM12Dec 21, 2022
AIPL11Nov 19, 2024
AIRE2Nov 19, 2024
AK21Jul 18, 2024
AKAP91Jul 18, 2024
AKT11Dec 21, 2022
AKT31Jul 18, 2024
ALAS22Nov 19, 2024
ALDH18A14Nov 19, 2024
ALDH3A21Nov 19, 2024
ALDH5A12Jul 18, 2024
ALDH6A11Jul 18, 2024
ALDH7A15Nov 19, 2024
ALDOB3Dec 21, 2022
ALG15Jul 18, 2024
ALG132Nov 19, 2024
ALG21Dec 21, 2022
ALG33Jul 18, 2024
ALG61Jul 18, 2024
ALG83Nov 19, 2024
ALG94Nov 19, 2024
ALKBH81Jul 18, 2024
ALMS18Jul 18, 2024
ALOXE32Jul 18, 2024
ALPK11Jul 18, 2024
ALPK325Nov 19, 2024
ALPL8Nov 19, 2024
ALS23Dec 21, 2022
AMER11Nov 19, 2024
AMH2Nov 19, 2024
AMPD22Aug 30, 2020
AMT2Jul 18, 2024
ANK27Nov 19, 2024
ANK34Nov 19, 2024
ANKLE21Jul 18, 2024
ANKRD11Dec 21, 2022
ANKRD1134Nov 19, 2024
ANKRD173Nov 19, 2024
ANKRD263Jul 18, 2024
ANLN2Dec 21, 2022
ANO103Dec 21, 2022
ANO31Jul 18, 2024
ANO55Nov 19, 2024
ANOS13Nov 19, 2024
AOPEP1Dec 21, 2022
AP1G12Nov 19, 2024
AP2M11Jul 18, 2024
AP3B21Nov 19, 2024
AP4B14Jul 18, 2024
AP4B1-AS13Jul 18, 2024
AP4M13Jul 18, 2024
AP4S11Jul 18, 2024
AP5Z15Nov 19, 2024
APC4Nov 19, 2024
APC29Nov 19, 2024
APOA51Nov 19, 2024
APOB10Nov 19, 2024
APOE1Nov 19, 2024
APP4Jul 18, 2024
AQP21Nov 19, 2024
AR14Nov 19, 2024
ARCN13Nov 19, 2024
ARF11Jul 18, 2024
ARFGEF14Nov 19, 2024
ARFGEF23Jul 18, 2024
ARFGEF31Dec 21, 2022
ARHGAP291Nov 19, 2024
ARHGAP312Dec 21, 2022
ARHGAP352Jul 18, 2024
ARHGEF181Dec 21, 2022
ARID1A7Nov 19, 2024
ARID1B27Nov 19, 2024
ARID25Jul 18, 2024
ARL61Dec 21, 2022
ARMC92Dec 21, 2022
ARSA6Jul 18, 2024
ARSB2Jul 18, 2024
ARSL2Dec 21, 2022
ARX1Nov 19, 2024
ASCC12Nov 19, 2024
ASH1L16Jul 18, 2024
ASL1Jul 18, 2024
ASNS1Jul 18, 2024
ASPA2Nov 19, 2024
ASPM16Nov 19, 2024
ASS13Jul 18, 2024
ASXL17Nov 19, 2024
ASXL24Nov 19, 2024
ASXL34Jul 18, 2024
ATAD3A4Nov 19, 2024
ATG4D1Nov 19, 2024
ATIC1Jul 18, 2024
ATL14Jul 18, 2024
ATL31Jul 18, 2024
ATM20Nov 19, 2024
ATP1A12Jul 18, 2024
ATP1A1-AS11Jul 18, 2024
ATP1A23Nov 19, 2024
ATP1A33Nov 19, 2024
ATP2B15Nov 19, 2024
ATP2B21Nov 19, 2024
ATP6AP23Nov 19, 2024
ATP6V0A12Nov 19, 2024
ATP6V0A21Jul 18, 2024
ATP6V0A41Nov 19, 2024
ATP6V1A4Nov 19, 2024
ATP6V1B13Jul 18, 2024
ATP6V1B23Nov 19, 2024
ATP7A9Nov 19, 2024
ATP7B13Nov 19, 2024
ATP8A21Dec 21, 2022
ATRIP8Nov 19, 2024
ATRIP-TREX18Nov 19, 2024
ATRX12Nov 19, 2024
ATXN7L3-AS12Nov 19, 2024
AUH1Jul 18, 2024
AUTS25Jul 18, 2024
AVP1Jul 18, 2024
AVPR25Nov 19, 2024
AXDND13Jul 18, 2024
B3GALNT22Dec 21, 2022
B3GALT62Jul 18, 2024
B4GALT71Dec 21, 2022
BAG37Nov 19, 2024
BAP12Nov 19, 2024
BAZ2B4Nov 19, 2024
BBOF11Jul 18, 2024
BBS12Nov 19, 2024
BBS103Dec 21, 2022
BBS24Jul 18, 2024
BBS51Jul 18, 2024
BBS72Dec 21, 2022
BBS92Dec 21, 2022
BCAP311Jul 18, 2024
BCHE4Nov 19, 2024
BCKDHB2Dec 21, 2022
BCL11A4Nov 19, 2024
BCL11B6Nov 19, 2024
BCOR3Jul 18, 2024
BCORL16Nov 19, 2024
BCS1L4Nov 19, 2024
BEST15Nov 19, 2024
BGN2Nov 19, 2024
BICD22Nov 19, 2024
BICRA1Dec 21, 2022
BIVM-ERCC53Dec 21, 2022
BLM2Jul 18, 2024
BLOC1S1-RDH51Dec 21, 2022
BLTP15Dec 21, 2022
BMP22Jul 18, 2024
BMP42Jul 18, 2024
BMPR24Jul 18, 2024
BNC21Nov 19, 2024
BOLA31Oct 1, 2019
BPTF9Nov 19, 2024
BRAF7Jul 18, 2024
BRAT19Nov 19, 2024
BRCA110Nov 19, 2024
BRCA28Nov 19, 2024
BRD42Jul 18, 2024
BRF11Dec 21, 2022
BRIP14Nov 19, 2024
BRPF112Nov 19, 2024
BRWD34Nov 19, 2024
BSCL23Nov 19, 2024
BSN2Nov 19, 2024
BTD4Nov 19, 2024
BTK3Nov 19, 2024
BUB1B2Dec 21, 2022
C10orf1051Dec 21, 2022
C11orf6511Nov 19, 2024
C14orf391Jul 18, 2024
C17orf1071Nov 19, 2024
C19orf123Nov 19, 2024
C1GALT1C11Nov 19, 2024
C1QA1Dec 21, 2022
C1R2Nov 19, 2024
C1orf1052Nov 19, 2024
C2CD32Dec 21, 2022
C31Nov 19, 2024
C61Jul 18, 2024
C71Jul 18, 2024
C8B1Nov 19, 2024
C91Nov 19, 2024
CABP41Dec 21, 2022
CACNA1A23Nov 19, 2024
CACNA1C21Nov 19, 2024
CACNA1C-AS17Jul 18, 2024
CACNA1D4Nov 19, 2024
CACNA1E7Nov 19, 2024
CACNA1F3Nov 19, 2024
CACNA1G7Nov 19, 2024
CACNA1H3Jul 18, 2024
CACNA1S3Nov 19, 2024
CACNA2D11Dec 21, 2022
CACNA2D21Dec 21, 2022
CACNB22Dec 21, 2022
CAD8Nov 19, 2024
CALM11Nov 19, 2024
CALM21Dec 21, 2022
CALM32Jul 18, 2024
CALR31Dec 21, 2022
CAMK2A2Dec 21, 2022
CAMK2B3Jul 18, 2024
CAMK2D1Nov 19, 2024
CAMTA14Nov 19, 2024
CANT11Jul 18, 2024
CAPN11Dec 21, 2022
CAPN151Nov 19, 2024
CAPN310Nov 19, 2024
CARD142Dec 21, 2022
CARD91Aug 3, 2022
CARS12Jul 18, 2024
CARS23Nov 19, 2024
CASD11Nov 19, 2024
CASK10Nov 19, 2024
CASQ25Nov 19, 2024
CASR9Nov 19, 2024
CAST1Nov 19, 2024
CAV31Nov 19, 2024
CBL4Nov 19, 2024
CBS4Nov 19, 2024
CC2D1A1Jul 18, 2024
CC2D2A9Nov 19, 2024
CCBE11Jul 18, 2024
CCDC1071Jul 18, 2024
CCDC1152Jul 18, 2024
CCDC224Nov 19, 2024
CCDC392Dec 21, 2022
CCDC402Nov 19, 2024
CCDC501Dec 21, 2022
CCDC651Dec 21, 2022
CCDST17Nov 19, 2024
CCN62Jul 18, 2024
CCND23Jul 18, 2024
CCNF2Nov 19, 2024
CCNH7Jul 18, 2024
CD40LG1Nov 19, 2024
CD461Nov 19, 2024
CD631Dec 21, 2022
CDAN12Dec 21, 2022
CDH11Jul 18, 2024
CDH112Nov 19, 2024
CDH2312Nov 19, 2024
CDK137Jul 18, 2024
CDK191Dec 21, 2022
CDK83Nov 19, 2024
CDKL59Nov 19, 2024
CDON2Jul 18, 2024
CELF21Nov 19, 2024
CENPE1Dec 21, 2022
CEP1043Nov 19, 2024
CEP1351Dec 21, 2022
CEP29011Nov 19, 2024
CEP411Jul 18, 2024
CEP831Nov 19, 2024
CEP85L3Nov 19, 2024
CERKL2Dec 21, 2022
CERS13Nov 19, 2024
CERT11Nov 19, 2024
CFAP2982Nov 19, 2024
CFAP298-TCP10L2Nov 19, 2024
CFAP4102Nov 19, 2024
CFAP921Jul 18, 2024
CFAP961Nov 19, 2024
CFH3Nov 19, 2024
CFHR11Nov 19, 2024
CFI1Apr 4, 2023
CFTR2Apr 4, 2023
CFTR-AS11Oct 1, 2019
CHAMP11Jul 18, 2024
CHAT2Dec 21, 2022
CHCHD101Nov 19, 2024
CHD16Nov 19, 2024
CHD211Jul 18, 2024
CHD314Nov 19, 2024
CHD416Nov 19, 2024
CHD56Nov 19, 2024
CHD728Nov 19, 2024
CHD811Jul 18, 2024
CHM5Nov 19, 2024
CHMP1A1Nov 19, 2024
CHRDL12Jul 18, 2024
CHRNA41Jul 18, 2024
CHRNB11Nov 19, 2024
CHRNE1Nov 19, 2024
CHST31Jul 18, 2024
CHST61Jul 18, 2024
CIC9Nov 19, 2024
CIT2Dec 21, 2022
CITED21Dec 21, 2022
CKAP2L2Jul 18, 2024
CLASP16Nov 19, 2024
CLCN15Nov 19, 2024
CLCN22Nov 19, 2024
CLCN31Nov 19, 2024
CLCN44Nov 19, 2024
CLCN512Nov 19, 2024
CLCN62Jul 18, 2024
CLCN71Nov 19, 2024
CLCNKB2Dec 21, 2022
CLDN141Dec 21, 2022
CLDN14-AS11Dec 21, 2022
CLDN161Aug 30, 2020
CLDN191Jul 18, 2024
CLDN51Nov 19, 2024
CLN32Jul 18, 2024
CLPB3Nov 19, 2024
CLTC5Nov 19, 2024
CNGA32Dec 21, 2022
CNGB35Jul 18, 2024
CNKSR11Dec 21, 2022
CNKSR21Nov 19, 2024
CNNM21Nov 19, 2024
CNOT15Nov 19, 2024
CNOT22Jul 18, 2024
CNOT33Jul 18, 2024
CNPY31Dec 21, 2022
CNPY3-GNMT2Jul 18, 2024
CNTNAP12Nov 19, 2024
CNTNAP23Jul 18, 2024
COASY2Jul 18, 2024
COCH4Nov 19, 2024
COG41Nov 19, 2024
COG61Dec 21, 2022
COG82Dec 21, 2022
COL10A13Jul 18, 2024
COL11A110Nov 19, 2024
COL11A23Nov 19, 2024
COL12A19Nov 19, 2024
COL13A12Nov 19, 2024
COL18A11Nov 19, 2024
COL1A123Nov 19, 2024
COL1A213Nov 19, 2024
COL25A12Jul 18, 2024
COL27A11Dec 21, 2022
COL2A123Nov 19, 2024
COL3A112Nov 19, 2024
COL4A117Nov 19, 2024
COL4A29Nov 19, 2024
COL4A2-AS13Nov 19, 2024
COL4A2-AS21Dec 21, 2022
COL4A367Nov 19, 2024
COL4A480Nov 19, 2024
COL4A564Nov 19, 2024
COL4A61Nov 19, 2024
COL5A110Nov 19, 2024
COL5A26Nov 19, 2024
COL6A13Nov 19, 2024
COL6A21Nov 19, 2024
COL6A313Nov 19, 2024
COL7A119Nov 19, 2024
COL9A13Nov 19, 2024
COL9A23Nov 19, 2024
COL9A34Nov 19, 2024
COLQ4Nov 19, 2024
COPB21Nov 19, 2024
COQ72Nov 19, 2024
COQ8A1Nov 19, 2024
COX153Dec 21, 2022
COX202Nov 19, 2024
CP2Nov 19, 2024
CPEB1-AS11Nov 19, 2024
CPLANE115Nov 19, 2024
CPOX1Nov 19, 2024
CPS17Nov 19, 2024
CPT1C1Jul 18, 2024
CPT22Nov 19, 2024
CRB14Nov 19, 2024
CRB22Jul 18, 2024
CREBBP21Nov 19, 2024
CRPPA3Nov 19, 2024
CRPPA-AS11Dec 21, 2022
CRTAP2Dec 21, 2022
CRY11Jul 18, 2024
CRYAB1Nov 19, 2024
CRYBB21Jul 18, 2024
CRYGS1Dec 21, 2022
CRYM1Dec 21, 2022
CSDE11Dec 21, 2022
CSF1R2Nov 19, 2024
CSF3R1Dec 21, 2022
CSGALNACT11Dec 21, 2022
CSNK1G11Nov 19, 2024
CSNK2A13Nov 19, 2024
CSNK2B5Nov 19, 2024
CSPP11Jul 18, 2024
CSRP38Nov 19, 2024
CTC12Nov 19, 2024
CTCF6Nov 19, 2024
CTDP11Dec 21, 2022
CTNNA21Dec 21, 2022
CTNNA32Dec 21, 2022
CTNNB114Jul 18, 2024
CTNND13Nov 19, 2024
CTNND21Dec 21, 2022
CTNS1Apr 4, 2023
CTR92Nov 19, 2024
CTSA2Nov 19, 2024
CTSD1Jul 18, 2024
CUBN10Nov 19, 2024
CUL36Nov 19, 2024
CUL4B5Nov 19, 2024
CUX14Nov 19, 2024
CUX23Jul 18, 2024
CYBB3Nov 19, 2024
CYFIP21Nov 19, 2024
CYP11A11Dec 21, 2022
CYP11B12Nov 19, 2024
CYP17A11Nov 19, 2024
CYP19A11Nov 19, 2024
CYP1B14Jul 18, 2024
CYP21A210Jul 18, 2024
CYP24A11Jul 18, 2024
CYP27A12Dec 21, 2022
CYP2U12Jul 18, 2024
CYP4V21Dec 21, 2022
CYP7B11Dec 21, 2022
CZ1P-ASNS1Jul 18, 2024
D2HGDH2Dec 21, 2022
DAG12Jul 18, 2024
DARS13Nov 19, 2024
DARS25Nov 19, 2024
DBR12Nov 19, 2024
DCC3Nov 19, 2024
DCHS12Nov 19, 2024
DCTN11Nov 19, 2024
DCX3Nov 19, 2024
DDB11Jul 18, 2024
DDC4Dec 21, 2022
DDHD11Jul 18, 2024
DDHD21Jul 18, 2024
DDR21Nov 19, 2024
DDX115Nov 19, 2024
DDX232Jul 18, 2024
DDX3X11Nov 19, 2024
DDX411Nov 19, 2024
DDX63Nov 19, 2024
DEAF15Nov 19, 2024
DEPDC511Nov 19, 2024
DES5Nov 19, 2024
DHCR711Nov 19, 2024
DHDDS2Nov 19, 2024
DHH1Dec 21, 2022
DHPS2Nov 19, 2024
DHTKD12Nov 19, 2024
DHX161Dec 21, 2022
DHX303Nov 19, 2024
DHX374Nov 19, 2024
DIAPH12Nov 19, 2024
DIP2B1Dec 21, 2022
DIPK1A4Jul 18, 2024
DIS3L22Dec 21, 2022
DKC15Nov 19, 2024
DLAT1Nov 19, 2024
DLD1Dec 21, 2022
DLG33Nov 19, 2024
DLG3-AS11Jul 18, 2024
DLG48Nov 19, 2024
DLL13Nov 19, 2024
DLL41Jul 18, 2024
DMD22Nov 19, 2024
DMP11Nov 19, 2024
DMXL21Nov 19, 2024
DNA21Nov 19, 2024
DNAAF42Nov 19, 2024
DNAAF4-CCPG12Nov 19, 2024
DNAH11Nov 19, 2024
DNAH118Jul 18, 2024
DNAH55Jul 18, 2024
DNAH92Jul 18, 2024
DNAI13Nov 19, 2024
DNAJB113Nov 19, 2024
DNAJB131Nov 19, 2024
DNAJB21Nov 19, 2024
DNAJC213Jul 18, 2024
DNM13Nov 19, 2024
DNM1L3Nov 19, 2024
DNM24Nov 19, 2024
DNMBP1Jul 18, 2024
DNMBP-AS11Jul 18, 2024
DNMT16Nov 19, 2024
DNMT3A9Nov 19, 2024
DOCK61Nov 19, 2024
DOCK6-AS11Nov 19, 2024
DOCK74Jul 18, 2024
DOK71Dec 21, 2022
DONSON4Nov 19, 2024
DPF23Nov 19, 2024
DPM11Dec 21, 2022
DPYD8Dec 21, 2022
DPYD-AS12Dec 21, 2022
DPYS2Nov 19, 2024
DSC23Nov 19, 2024
DSCAM1Nov 19, 2024
DSG11Nov 19, 2024
DSG1-AS12Nov 19, 2024
DSG221Nov 19, 2024
DSG2-AS16Nov 19, 2024
DSG41Dec 21, 2022
DSP40Nov 19, 2024
DSPP1Nov 19, 2024
DST1Dec 21, 2022
DTNA1Jul 18, 2024
DUOX22Nov 19, 2024
DUOXA21Dec 21, 2022
DUSP291Nov 19, 2024
DVL13Jul 18, 2024
DVL31Nov 19, 2024
DYNC1H111Nov 19, 2024
DYNC2H111Nov 19, 2024
DYNC2LI13Jul 18, 2024
DYRK1A9Jul 18, 2024
DYSF3Dec 21, 2022
DZIP1L2Jul 18, 2024
EARS24Jul 18, 2024
EBF34Nov 19, 2024
EBP2Nov 19, 2024
ECEL15Jul 18, 2024
ECHS111Nov 19, 2024
EDA7Nov 19, 2024
EDAR1Nov 19, 2024
EDNRB3Nov 19, 2024
EDNRB-AS12Nov 19, 2024
EED1Jul 18, 2024
EEF1A26Jul 18, 2024
EEF1D2Dec 21, 2022
EEF22Jul 18, 2024
EEF2KMT1Jul 18, 2024
EFEMP11Nov 19, 2024
EFEMP22Jul 18, 2024
EFL11Jul 18, 2024
EFNB13Nov 19, 2024
EFTUD210Nov 19, 2024
EGR22Nov 19, 2024
EHBP1L11Nov 19, 2024
EHMT19Nov 19, 2024
EIF2B11Dec 21, 2022
EIF2B24Nov 19, 2024
EIF2B31Dec 21, 2022
EIF2B43Nov 19, 2024
EIF2B52Dec 21, 2022
EIF3F1Nov 19, 2024
ELAC22Nov 19, 2024
ELANE3Nov 19, 2024
ELN5Nov 19, 2024
ELN-AS12Dec 21, 2022
ELOVL41Nov 19, 2024
ELOVL51Dec 21, 2022
ELP11Nov 19, 2024
ELP22Dec 21, 2022
EMC15Nov 19, 2024
EMC1-AS15Nov 19, 2024
EMD2Jul 18, 2024
EME21Dec 21, 2022
EMILIN11Nov 19, 2024
EML12Dec 21, 2022
ENAM1Nov 19, 2024
ENG16Nov 19, 2024
ENO32Dec 21, 2022
ENPP12Oct 1, 2019
EP30011Nov 19, 2024
EPAS12Jul 18, 2024
EPB41L11Dec 21, 2022
EPHA22Nov 19, 2024
EPHB411Nov 19, 2024
EPHX11Nov 19, 2024
EPRS12Dec 21, 2022
ERCC12Sep 16, 2020
ERCC22Nov 19, 2024
ERCC33Jul 18, 2024
ERCC42Dec 21, 2022
ERCC53Dec 21, 2022
ERCC68Nov 19, 2024
ERCC82Nov 19, 2024
ERF4Nov 19, 2024
ESPN1Nov 19, 2024
ESRRB1Dec 21, 2022
ETFA2Nov 19, 2024
ETFB1Dec 21, 2022
ETFDH4Jul 18, 2024
ETHE13Jul 18, 2024
ETV62Jul 18, 2024
EVC23Nov 19, 2024
EXOC71Dec 21, 2022
EXOSC33Jul 18, 2024
EXOSC91Jul 18, 2024
EXPH51Dec 21, 2022
EXT12Nov 19, 2024
EXT22Nov 19, 2024
EYA14Nov 19, 2024
EYA42Jul 18, 2024
EYS4Jul 18, 2024
EZH23Nov 19, 2024
F116Nov 19, 2024
F11-AS11Nov 19, 2024
F13B1Jul 18, 2024
F23Nov 19, 2024
F53Nov 19, 2024
F72Jul 18, 2024
F810Nov 19, 2024
F91Dec 21, 2022
FA2H2Dec 21, 2022
FAH1Jul 18, 2024
FAM111A4Nov 19, 2024
FAM20A1Dec 21, 2022
FAN16Nov 19, 2024
FANCA7Nov 19, 2024
FANCB1Jul 18, 2024
FANCC2Jul 18, 2024
FANCD24Nov 19, 2024
FANCG1Dec 21, 2022
FANCI1Nov 19, 2024
FANCL2Nov 19, 2024
FAR11Nov 19, 2024
FAS1Nov 19, 2024
FASTKD21Nov 19, 2024
FAT14Nov 19, 2024
FAT21Nov 19, 2024
FAT47Jul 18, 2024
FBLN11Nov 19, 2024
FBN153Nov 19, 2024
FBN217Nov 19, 2024
FBXL45Nov 19, 2024
FBXO113Nov 19, 2024
FBXO281Nov 19, 2024
FBXO311Nov 19, 2024
FBXW73Nov 19, 2024
FDFT11Dec 21, 2022
FDXR3Jul 18, 2024
FECH4Nov 19, 2024
FEM1C2Nov 19, 2024
FERRY32Jul 18, 2024
FEZF21Nov 19, 2024
FGA1Nov 19, 2024
FGD16Jul 18, 2024
FGF102Nov 19, 2024
FGF141Jul 18, 2024
FGF33Nov 19, 2024
FGF91Dec 21, 2022
FGFR15Nov 19, 2024
FGFR27Nov 19, 2024
FGFR311Nov 19, 2024
FH3Nov 19, 2024
FHL12Nov 19, 2024
FHOD315Nov 19, 2024
FKBP101Dec 21, 2022
FKRP5Nov 19, 2024
FKTN4Jul 18, 2024
FLCN2Nov 19, 2024
FLG17Nov 19, 2024
FLII1Jul 18, 2024
FLNA13Nov 19, 2024
FLNB3Nov 19, 2024
FLNC52Nov 19, 2024
FLNC-AS119Nov 19, 2024
FLT47Nov 19, 2024
FLVCR12Nov 19, 2024
FMN23Dec 21, 2022
FMO31Jul 18, 2024
FMR11Jul 18, 2024
FN19Nov 19, 2024
FOLR11Jul 18, 2024
FOXC11Jul 18, 2024
FOXC21Dec 21, 2022
FOXC2-AS11Dec 21, 2022
FOXE11Nov 19, 2024
FOXE31Nov 19, 2024
FOXF11Jul 18, 2024
FOXG15Jul 18, 2024
FOXL22Jul 18, 2024
FOXP117Nov 19, 2024
FOXP25Jul 18, 2024
FOXP31Dec 21, 2022
FOXP42Nov 19, 2024
FOXRED13Dec 21, 2022
FPGT-TNNI3K3Jul 18, 2024
FRAS12Nov 19, 2024
FREM22Jul 18, 2024
FRMD51Jul 18, 2024
FRMD73Nov 19, 2024
FRMPD41Jul 18, 2024
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NR0B14Nov 19, 2024
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PAX22Nov 19, 2024
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PIDD12Jul 18, 2024
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PLEC1Nov 19, 2024
PLN2Nov 19, 2024
PLOD21Nov 19, 2024
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PLP13Nov 19, 2024
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PLS32Nov 19, 2024
PLXNA12Nov 19, 2024
PMM211Nov 19, 2024
PMPCB3Dec 21, 2022
PMS22Nov 19, 2024
PNKD1Dec 21, 2022
PNKP4Nov 19, 2024
PNP1Jul 18, 2024
PNPLA23Jul 18, 2024
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PNPO3Nov 19, 2024
PNPT15Nov 19, 2024
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POC1B1Dec 21, 2022
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POLA13Nov 19, 2024
POLD12Nov 19, 2024
POLE4Nov 19, 2024
POLG25Nov 19, 2024
POLG21Nov 19, 2024
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POLR1B1Dec 21, 2022
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POLRMT2Nov 19, 2024
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POR3Jul 18, 2024
PORCN1Jul 18, 2024
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POU4F32Dec 21, 2022
PPA26Jul 18, 2024
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PPP2R1A1Jul 18, 2024
PPP2R5D5Jul 18, 2024
PPP3CA1Dec 21, 2022
PPT14Nov 19, 2024
PQBP11Nov 19, 2024
PRDM163Jul 18, 2024
PRDM61Nov 19, 2024
PREPL2Nov 19, 2024
PRF13Jul 18, 2024
PRICKLE11Nov 19, 2024
PRKACB1Dec 21, 2022
PRKAG23Jul 18, 2024
PRKAR1A1Dec 21, 2022
PRKCG1Jul 18, 2024
PRKCSH3Nov 19, 2024
PRKD12Dec 21, 2022
PRKDC1Dec 21, 2022
PRKG11Jul 18, 2024
PRKN3Jul 18, 2024
PRMT72Jul 18, 2024
PROC4Nov 19, 2024
PROKR23Nov 19, 2024
PROS13Nov 19, 2024
PRPF314Nov 19, 2024
PRPF31-AS12Nov 19, 2024
PRPF42Dec 21, 2022
PRPF83Nov 19, 2024
PRPH22Nov 19, 2024
PRPS11Nov 19, 2024
PRR123Jul 18, 2024
PRRT27Nov 19, 2024
PRRX11Nov 19, 2024
PRUNE11Nov 19, 2024
PRX1Nov 19, 2024
PSAT12Dec 21, 2022
PSEN18Nov 19, 2024
PSEN21Jul 18, 2024
PSMC32Nov 19, 2024
PSMC51Nov 19, 2024
PSMD121Nov 19, 2024
PSMF11Nov 19, 2024
PSTPIP11Dec 21, 2022
PTCH17Jul 18, 2024
PTCHD11Nov 19, 2024
PTCHD1-AS4Nov 19, 2024
PTEN26Nov 19, 2024
PTF1A1Apr 4, 2023
PTH1R1Nov 19, 2024
PTPN1134Nov 19, 2024
PTPN234Jul 18, 2024
PTPN42Jul 18, 2024
PTPRQ8Nov 19, 2024
PTS2Nov 19, 2024
PUF6011Nov 19, 2024
PUM12Nov 19, 2024
PURA10Nov 19, 2024
PUS33Jul 18, 2024
PUS71Jul 18, 2024
PYGM4Dec 21, 2022
QARS12Dec 21, 2022
QRICH14Jul 18, 2024
QRSL11Jul 18, 2024
RAB11B3Jul 18, 2024
RAB231Jul 18, 2024
RAB33A2Dec 21, 2022
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RAC13Nov 19, 2024
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RAD212Nov 19, 2024
RAD512Jul 18, 2024
RAD51C1Jul 18, 2024
RAD51D1Dec 21, 2022
RAD51L3-RFFL1Dec 21, 2022
RAF112Nov 19, 2024
RAG22Nov 19, 2024
RAI13Jul 18, 2024
RALA2Jul 18, 2024
RANBP23Nov 19, 2024
RAP1B1Nov 19, 2024
RAPSN3Jul 18, 2024
RARB3Nov 19, 2024
RARS13Jul 18, 2024
RARS26Nov 19, 2024
RASA17Jul 18, 2024
RB13Nov 19, 2024
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RDH51Dec 21, 2022
RECQL44Dec 21, 2022
REEP11Jul 18, 2024
RELN5Nov 19, 2024
REN1Nov 19, 2024
RERE12Jul 18, 2024
RET6Nov 19, 2024
RFT12Jul 18, 2024
RFX31Nov 19, 2024
RFX71Nov 19, 2024
RHO4Nov 19, 2024
RHOBTB23Jul 18, 2024
RIC12Jul 18, 2024
RIF16Jul 18, 2024
RIMS11Dec 21, 2022
RIT18Jul 18, 2024
RLIG11Jul 18, 2024
RLIM2Nov 19, 2024
RMRP4Jul 18, 2024
RNASEH2A2Dec 21, 2022
RNASEH2B1Jul 18, 2024
RNASEH2C3Jul 18, 2024
RNF1251Dec 21, 2022
RNF132Nov 19, 2024
RNF145Jul 18, 2024
RNF1701Nov 19, 2024
RNF2133Nov 19, 2024
RNF213-AS12Nov 19, 2024
RNF2161Dec 21, 2022
RNF2201Jul 18, 2024
RNU4-11Nov 19, 2024
RNU4-21Nov 19, 2024
RNU4ATAC6Nov 19, 2024
ROBO33Dec 21, 2022
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RORB1Jul 18, 2024
RP11Nov 19, 2024
RP1L13Nov 19, 2024
RP21Nov 19, 2024
RPE651Nov 19, 2024
RPGR3Nov 19, 2024
RPGRIP13Jul 18, 2024
RPGRIP1L5Nov 19, 2024
RPL152Nov 19, 2024
RPL36A-HNRNPH28Nov 19, 2024
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RS12Dec 21, 2022
RSPH4A1Dec 21, 2022
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RTEL1-TNFRSF6B9Nov 19, 2024
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RTTN8Nov 19, 2024
RUNX12Nov 19, 2024
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RUNX22Jul 18, 2024
RUSF11Nov 19, 2024
RXYLT11Dec 21, 2022
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RYR234Nov 19, 2024
SACS4Jul 18, 2024
SAG1Jul 18, 2024
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SAMD9L2Nov 19, 2024
SAMHD12Jul 18, 2024
SAR1B1Jul 18, 2024
SARM12Jul 18, 2024
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SBDS4Nov 19, 2024
SBF12Jul 18, 2024
SCAF42Jul 18, 2024
SCAMP41Nov 19, 2024
SCN11A2Nov 19, 2024
SCN1A24Nov 19, 2024
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SCO24Nov 19, 2024
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SEC61A12Nov 19, 2024
SEC637Nov 19, 2024
SEMA4A1Nov 19, 2024
SEMA6B1Jul 18, 2024
SERPINA14Nov 19, 2024
SET1Jul 18, 2024
SETBP111Nov 19, 2024
SETD1A1Dec 21, 2022
SETD1B11Nov 19, 2024
SETD211Nov 19, 2024
SETD518Nov 19, 2024
SETX4Nov 19, 2024
SF3B21Jul 18, 2024
SFTA31Dec 21, 2022
SFTPC2Nov 19, 2024
SGCB1Nov 19, 2024
SGCE2Nov 19, 2024
SGPL12Jul 18, 2024
SGSH4Jul 18, 2024
SH2B31Dec 21, 2022
SH2D1A1Nov 19, 2024
SH3TC25Nov 19, 2024
SHANK12Nov 19, 2024
SHANK26Nov 19, 2024
SHANK32Nov 19, 2024
SHH5Nov 19, 2024
SHOC22Jul 18, 2024
SHQ11Jul 18, 2024
SHROOM41Nov 19, 2024
SI2Nov 19, 2024
SIGMAR12Jul 18, 2024
SIM11Jul 18, 2024
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SIX11Dec 21, 2022
SIX61Jul 18, 2024
SKI6Nov 19, 2024
SKIC21Dec 21, 2022
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SLC2A103Nov 19, 2024
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SLC34A16Nov 19, 2024
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SLC39A81Dec 21, 2022
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SLC4A31Jul 18, 2024
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SLC5A62Dec 21, 2022
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SLC6A92Nov 19, 2024
SLC7A97Nov 19, 2024
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SLX42Dec 21, 2022
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SMAD46Nov 19, 2024
SMAD63Jul 18, 2024
SMARCA213Nov 19, 2024
SMARCA45Nov 19, 2024
SMARCA52Nov 19, 2024
SMARCAL12Dec 21, 2022
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SMARCC21Nov 19, 2024
SMARCD13Nov 19, 2024
SMARCE11Jul 18, 2024
SMC1A7Nov 19, 2024
SMC31Dec 21, 2022
SMCHD11Nov 19, 2024
SMN17Nov 19, 2024
SMN21Dec 21, 2022
SMO1Dec 21, 2022
SMPD11Jul 18, 2024
SMPD43Dec 21, 2022
SMS1Jul 18, 2024
SNAP251Jul 18, 2024
SNCA2Nov 19, 2024
SNHG144Nov 19, 2024
SNHG222Jul 18, 2024
SNHG311Dec 21, 2022
SNRNP2003Nov 19, 2024
SNRPB1Jul 18, 2024
SOD13Nov 19, 2024
SON13Nov 19, 2024
SORD2Jul 18, 2024
SOS111Nov 19, 2024
SOS24Jul 18, 2024
SOX112Nov 19, 2024
SOX32Nov 19, 2024
SOX43Nov 19, 2024
SOX54Nov 19, 2024
SOX63Jul 18, 2024
SOX92Jul 18, 2024
SP1101Jul 18, 2024
SP1401Jul 18, 2024
SPAST17Nov 19, 2024
SPATA222Nov 19, 2024
SPATA72Dec 21, 2022
SPECC1L1Nov 19, 2024
SPECC1L-ADORA2A1Nov 19, 2024
SPEG1Dec 21, 2022
SPEN5Jul 18, 2024
SPG1117Nov 19, 2024
SPG211Jul 18, 2024
SPG77Nov 19, 2024
SPINK54Jul 18, 2024
SPINT21Jul 18, 2024
SPR3Nov 19, 2024
SPRED15Nov 19, 2024
SPTA12Nov 19, 2024
SPTAN18Nov 19, 2024
SPTB2Oct 1, 2019
SPTBN18Nov 19, 2024
SPTBN22Nov 19, 2024
SPTBN44Jul 18, 2024
SPTLC11Jul 18, 2024
SPTLC21Jul 18, 2024
SQSTM12Nov 19, 2024
SRCAP4Nov 19, 2024
SRD5A25Jul 18, 2024
SRD5A32Nov 19, 2024
SRD5A3-AS12Nov 19, 2024
SRFBP11Jul 18, 2024
SRP541Nov 19, 2024
SRPX21Jul 18, 2024
SRRM24Nov 19, 2024
SRSF11Nov 19, 2024
SSR42Nov 19, 2024
STAG14Jul 18, 2024
STAG23Nov 19, 2024
STAMBP2Nov 19, 2024
STAT11Nov 1, 2016
STEEP12Nov 19, 2024
STING12Nov 19, 2024
STON1-GTF2A1L1Nov 19, 2024
STRC4Nov 19, 2024
STT3A2Nov 19, 2024
STUB15Nov 19, 2024
STX111Dec 21, 2022
STXBP116Nov 19, 2024
SUCLG11Dec 21, 2022
SUFU4Nov 19, 2024
SUPT16H3Nov 19, 2024
SURF13Nov 19, 2024
SUZ121Jul 18, 2024
SYNE113Nov 19, 2024
SYNE1-AS11Nov 19, 2024
SYNE21Dec 21, 2022
SYNGAP115Nov 19, 2024
SYNGAP1-AS111Nov 19, 2024
SYP1Nov 19, 2024
SYT11Nov 19, 2024
SZT27Jul 18, 2024
SZT2-AS11Dec 21, 2022
TAB24Nov 19, 2024
TAF15Nov 19, 2024
TAF23Dec 21, 2022
TAF43Nov 19, 2024
TAFAZZIN5Nov 19, 2024
TANC25Nov 19, 2024
TANGO24Jul 18, 2024
TAOK16Nov 19, 2024
TAPBPL1Dec 21, 2022
TARID1Dec 21, 2022
TARS24Nov 19, 2024
TBC1D11Aug 3, 2022
TBC1D246Nov 19, 2024
TBC1D321Jul 18, 2024
TBC1D7-LOC1001303573Nov 19, 2024
TBC1D8B1Nov 19, 2024
TBCD8Jul 18, 2024
TBCE1Dec 21, 2022
TBCEL-TECTA14Nov 19, 2024
TBCK2Jul 18, 2024
TBK12Jul 18, 2024
TBL1XR15Nov 19, 2024
TBL1XR1-AS12Jul 18, 2024
TBR13Nov 19, 2024
TBX11Jul 18, 2024
TBX181Nov 19, 2024
TBX191Jul 18, 2024
TBX201Jul 18, 2024
TBX41Nov 19, 2024
TBX56Nov 19, 2024
TCEAL11Nov 19, 2024
TCF125Nov 19, 2024
TCF207Nov 19, 2024
TCF31Nov 19, 2024
TCF413Nov 19, 2024
TCIRG13Nov 19, 2024
TCOF17Jul 18, 2024
TCTN12Dec 21, 2022
TCTN33Dec 21, 2022
TECPR22Nov 19, 2024
TECRL6Nov 19, 2024
TECTA14Nov 19, 2024
TELO22Jul 18, 2024
TENM33Jul 18, 2024
TERT3Nov 19, 2024
TET21Jul 18, 2024
TET2-AS11Jul 18, 2024
TET37Nov 19, 2024
TFAP2A2Nov 19, 2024
TFAP2A-AS21Nov 19, 2024
TFAP2B1Dec 21, 2022
TFE31Nov 19, 2024
TFR21Dec 21, 2022
TGFB11Jul 18, 2024
TGFB24Jul 18, 2024
TGFB31Jul 18, 2024
TGFBR111Nov 19, 2024
TGFBR24Nov 19, 2024
TGIF11Dec 21, 2022
TGM13Jul 18, 2024
TGM54Jul 18, 2024
TH2Jul 18, 2024
THAP12Jul 18, 2024
THOC22Jul 18, 2024
THOC64Jul 18, 2024
THRA2Nov 19, 2024
THRB4Nov 19, 2024
THSD45Nov 19, 2024
THUMPD11Jul 18, 2024
TIMM501Nov 19, 2024
TINF23Jul 18, 2024
TJP22Nov 19, 2024
TK22Dec 21, 2022
TLK25Jul 18, 2024
TLL12Dec 21, 2022
TMC12Nov 19, 2024
TMEM106B1Dec 21, 2022
TMEM1382Nov 19, 2024
TMEM2372Jul 18, 2024
TMEM2401Dec 21, 2022
TMEM2601Dec 21, 2022
TMEM4313Jul 18, 2024
TMEM63A1Jul 18, 2024
TMEM673Jul 18, 2024
TMPPE1Dec 21, 2022
TMPRSS36Nov 19, 2024
TMX2-CTNND13Nov 19, 2024
TNC1Dec 21, 2022
TNFRSF13B2Nov 19, 2024
TNFRSF1A1Dec 21, 2022
TNK21Dec 21, 2022
TNNI21Dec 21, 2022
TNNI320Nov 19, 2024
TNNI3K3Jul 18, 2024
TNNT223Nov 19, 2024
TNPO31Dec 21, 2022
TNR2Dec 21, 2022
TNRC6B6Nov 19, 2024
TNS21Jul 18, 2024
TNXB7Nov 19, 2024
TOE12Jul 18, 2024
TOMT1Dec 21, 2022
TONSL2Dec 21, 2022
TOP3A5Nov 19, 2024
TOPORS1Dec 21, 2022
TP53BP11Jul 18, 2024
TP53RK2Jul 18, 2024
TP632Nov 19, 2024
TPM111Nov 19, 2024
TPM1-AS1Dec 21, 2022
TPO1Dec 21, 2022
TPP14Nov 19, 2024
TPP21Jul 18, 2024
TPRN1Dec 21, 2022
TRAF73Jul 18, 2024
TRAPPC124Jul 18, 2024
TRAPPC2L1Nov 19, 2024
TRAPPC41Dec 21, 2022
TRAPPC6B1Dec 21, 2022
TRAPPC95Jul 18, 2024
TRDN4Jul 18, 2024
TREX18Nov 19, 2024
TRIM634Nov 19, 2024
TRIM82Jul 18, 2024
TRIO17Nov 19, 2024
TRIOBP3Nov 19, 2024
TRIP111Dec 21, 2022
TRIP128Nov 19, 2024
TRIP132Dec 21, 2022
TRIT11Jul 18, 2024
TRMT10A1Nov 19, 2024
TRPC62Nov 19, 2024
TRPM35Nov 19, 2024
TRPM41Nov 19, 2024
TRPM63Nov 19, 2024
TRPS15Jul 18, 2024
TRPV41Jul 18, 2024
TRRAP16Nov 19, 2024
TSC17Nov 19, 2024
TSC214Nov 19, 2024
TSEN541Jul 18, 2024
TSFM3Jul 18, 2024
TSHR2Nov 19, 2024
TSPAN14Jul 18, 2024
TSPAN121Jul 18, 2024
TSPEAR3Nov 19, 2024
TSPEAR-AS11Dec 21, 2022
TSPOAP11Jul 18, 2024
TTC21B2Nov 19, 2024
TTC36-AS11Dec 21, 2022
TTC7A7Nov 19, 2024
TTI21Jul 18, 2024
TTN97Nov 19, 2024
TTN-AS161Nov 19, 2024
TTR3Nov 19, 2024
TUBA1A12Nov 19, 2024
TUBB2Jul 18, 2024
TUBB2A2Nov 19, 2024
TUBB2B1Jul 18, 2024
TUBB37Nov 19, 2024
TUBB4A2Jul 18, 2024
TUBGCP41Jul 18, 2024
TUBGCP66Nov 19, 2024
TUSC31Jul 18, 2024
TWIST13Nov 19, 2024
TWNK4Nov 19, 2024
TXNDC151Dec 21, 2022
TYMP5Nov 19, 2024
TYR10Nov 19, 2024
U2AF21Nov 19, 2024
UBA11Jul 18, 2024
UBA21Jul 18, 2024
UBA54Nov 19, 2024
UBAP2L2Nov 19, 2024
UBE2A2Jul 18, 2024
UBE3A4Nov 19, 2024
UBE3B2Dec 21, 2022
UBIAD11Nov 19, 2024
UBQLN22Jul 18, 2024
UBR11Dec 21, 2022
UBTF2Nov 19, 2024
UCHL11Nov 19, 2024
UFSP21Nov 19, 2024
UGDH2Nov 19, 2024
UGP21Jul 18, 2024
UMOD11Nov 19, 2024
UMPS2Nov 19, 2024
UNC13A2Nov 19, 2024
UNC13D2Nov 19, 2024
UNC45B1Nov 19, 2024
UNC791Nov 19, 2024
UNC806Jul 18, 2024
UPB11Nov 19, 2024
UPF11Dec 21, 2022
UPF3B5Nov 19, 2024
UROS2Nov 19, 2024
USB11Dec 21, 2022
USH1C7Nov 19, 2024
USH2A27Nov 19, 2024
USH2A-AS13Nov 19, 2024
USH2A-AS23Nov 19, 2024
USP27X1Nov 19, 2024
USP532Dec 21, 2022
USP73Nov 19, 2024
USP9X17Nov 19, 2024
VAC141Dec 21, 2022
VAMP11Dec 21, 2022
VARS11Nov 19, 2024
VARS24Jul 18, 2024
VCAN2Jul 18, 2024
VCAN-AS11Jul 18, 2024
VCL8Jul 18, 2024
VCP1Dec 21, 2022
VEGFC1Dec 21, 2022
VIM1Jul 18, 2024
VIM-AS11Jul 18, 2024
VIPAS392Nov 19, 2024
VLDLR1Jul 18, 2024
VMA211Nov 19, 2024
VPS112Dec 21, 2022
VPS13B10Jul 18, 2024
VPS13C2Dec 21, 2022
VPS13D6Nov 19, 2024
VPS37A1Dec 21, 2022
VRK21Nov 19, 2024
VWA11Jul 18, 2024
VWF11Nov 19, 2024
WAC2Nov 19, 2024
WARS21Dec 21, 2022
WAS3Jul 18, 2024
WASF12Nov 19, 2024
WASHC52Nov 19, 2024
WDFY311Nov 19, 2024
WDFY3-AS11Nov 19, 2024
WDPCP2Jul 18, 2024
WDR113Nov 19, 2024
WDR262Jul 18, 2024
WDR352Dec 21, 2022
WDR371Dec 21, 2022
WDR43Nov 19, 2024
WDR454Nov 19, 2024
WDR627Jul 18, 2024
WDR813Nov 19, 2024
WFS118Nov 19, 2024
WNK11Nov 19, 2024
WNK31Nov 19, 2024
WNT10A3Nov 19, 2024
WNT10B1Nov 19, 2024
WNT7A1Jul 18, 2024
WT16Nov 19, 2024
WWOX3Jul 18, 2024
XDH1Jul 18, 2024
XIAP1Nov 19, 2024
XPA2Dec 21, 2022
YARS21Nov 19, 2024
YWHAG1Jul 18, 2024
YY11Jul 18, 2024
YY1AP11Jul 18, 2024
ZBTB186Jul 18, 2024
ZBTB204Nov 19, 2024
ZBTB241Dec 21, 2022
ZBTB7A2Nov 19, 2024
ZC4H24Nov 19, 2024
ZDHHC241Jul 18, 2024
ZDHHC92Nov 19, 2024
ZEB25Nov 19, 2024
ZFHX37Nov 19, 2024
ZFHX3-AS16Nov 19, 2024
ZFHX44Nov 19, 2024
ZFX1Nov 19, 2024
ZFYVE268Jul 18, 2024
ZIC22Jul 18, 2024
ZIC34Nov 19, 2024
ZMIZ14Jul 18, 2024
ZMPSTE242Jul 18, 2024
ZMYM31Nov 19, 2024
ZMYND101Dec 21, 2022
ZMYND111Jul 18, 2024
ZMYND81Nov 19, 2024
ZNF1424Nov 19, 2024
ZNF1482Nov 19, 2024
ZNF2761Nov 19, 2024
ZNF29210Nov 19, 2024
ZNF3355Jul 18, 2024
ZNF4627Nov 19, 2024
ZNF4693Nov 19, 2024
ZNF6871Jul 18, 2024
ZNF6991Jul 18, 2024
ZNF7111Jul 18, 2024
ZSWIM61Dec 21, 2022

Condition

NameSubmissionsLast Updated
2-aminoadipic 2-oxoadipic aciduria2Nov 19, 2024
3-Methylglutaconic aciduria type 25Nov 19, 2024
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency5Jul 18, 2024
3-hydroxy-3-methylglutaryl-CoA synthase deficiency4Jul 18, 2024
3-methylcrotonyl-CoA carboxylase 2 deficiency1Jul 18, 2024
3-methylglutaconic aciduria type 11Jul 18, 2024
3-methylglutaconic aciduria, type VIIA1Nov 19, 2024
3-methylglutaconic aciduria, type VIIB2Nov 19, 2024
46,XX ovarian dysgenesis-short stature syndrome2Nov 19, 2024
46,XY sex reversal 112Nov 19, 2024
46,XY sex reversal 36Jul 18, 2024
46,XY sex reversal 64Nov 19, 2024
46,XY sex reversal 71Dec 21, 2022
5-Oxoprolinase deficiency2Nov 19, 2024
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency2Nov 19, 2024
8q24.3 microdeletion syndrome11Nov 19, 2024
ACCES syndrome1Jul 18, 2024
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder12Nov 19, 2024
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome7Nov 19, 2024
AIPL1-related retinopathy1Nov 19, 2024
ALDH18A1-related de Barsy syndrome1Nov 19, 2024
ALG1-congenital disorder of glycosylation5Jul 18, 2024
ALG2-congenital disorder of glycosylation1Dec 21, 2022
ALG3-congenital disorder of glycosylation3Jul 18, 2024
ALG6-congenital disorder of glycosylation 1C1Jul 18, 2024
ALG8 congenital disorder of glycosylation2Nov 19, 2024
ALG9 congenital disorder of glycosylation1Nov 19, 2024
ALG9-associated autosomal dominant polycystic kidney disease3Nov 19, 2024
AP-4 deficiency syndrome2Jul 18, 2024
AP4-related intellectual disability and spastic paraplegia1Dec 21, 2022
ATP1A3-associated neurological disorder3Nov 19, 2024
ATP6AP2-related disorder1Dec 21, 2022
ATR-X-related syndrome3Nov 19, 2024
Aarskog syndrome6Jul 18, 2024
Abetalipoproteinaemia2Nov 19, 2024
Abortive cerebellar ataxia1Nov 19, 2024
Achondrogenesis type II1Jul 18, 2024
Achondrogenesis, type IA1Dec 21, 2022
Achondroplasia2Nov 19, 2024
Achromatopsia 22Dec 21, 2022
Achromatopsia 35Jul 18, 2024
Achromatopsia 41Jul 18, 2024
Acral peeling skin syndrome4Jul 18, 2024
Acrocallosal syndrome1Jul 18, 2024
Acrocephalosyndactyly type I1Nov 19, 2024
Acrodysostosis 1 with or without hormone resistance1Dec 21, 2022
Acrofacial dysostosis Cincinnati type3Nov 19, 2024
Acromelic frontonasal dysostosis1Dec 21, 2022
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome1Jul 18, 2024
Acute intermittent porphyria2Jul 18, 2024
Acyl-CoA dehydrogenase 9 deficiency7Nov 19, 2024
Adams-Oliver syndrome 12Dec 21, 2022
Adams-Oliver syndrome 21Nov 19, 2024
Adams-Oliver syndrome 31Dec 21, 2022
Adams-Oliver syndrome 52Dec 21, 2022
Adams-Oliver syndrome 61Jul 18, 2024
Adenylosuccinate lyase deficiency2Jul 18, 2024
Adrenoleukodystrophy5Nov 19, 2024
Adult hypophosphatasia3Nov 19, 2024
Agammaglobulinemia 8, autosomal dominant1Nov 19, 2024
Aicardi-Goutieres syndrome 17Nov 19, 2024
Aicardi-Goutieres syndrome 21Jul 18, 2024
Aicardi-Goutieres syndrome 33Jul 18, 2024
Aicardi-Goutieres syndrome 42Dec 21, 2022
Aicardi-Goutieres syndrome 52Jul 18, 2024
Aicardi-Goutieres syndrome 63Nov 19, 2024
Aicardi-Goutieres syndrome 72Nov 19, 2024
Alagille syndrome due to a JAG1 point mutation9Nov 19, 2024
Alagille syndrome due to a NOTCH2 point mutation5Nov 19, 2024
Alazami-Yuan syndrome1Dec 21, 2022
Aldosterone-producing adenoma with seizures and neurological abnormalities2Nov 19, 2024
Alexander disease11Nov 19, 2024
Alkuraya-Kucinskas syndrome5Dec 21, 2022
Allan-Herndon-Dudley syndrome4Nov 19, 2024
Alopecia-intellectual disability syndrome 42Jul 18, 2024
Alpha thalassemia-X-linked intellectual disability syndrome7Nov 19, 2024
Alpha-1-antitrypsin deficiency4Nov 19, 2024
Alpha-N-acetylgalactosaminidase deficiency2Jul 18, 2024
Alpha-actinopathy2Nov 19, 2024
Alport syndrome131Nov 19, 2024
Alport syndrome 3b, autosomal recessive1Nov 19, 2024
Alstrom syndrome8Jul 18, 2024
Alveolar capillary dysplasia with pulmonary venous misalignment1Jul 18, 2024
Alzheimer disease1Nov 19, 2024
Alzheimer disease 35Nov 19, 2024
Alzheimer disease 41Jul 18, 2024
Alzheimer disease type 11Jul 18, 2024
Amelogenesis imperfecta - hypoplastic autosomal dominant - local1Nov 19, 2024
Amelogenesis imperfecta hypomaturation type 2A22Nov 19, 2024
Amelogenesis imperfecta, hypomaturation type, IIa61Dec 21, 2022
Aminoacylase 1 deficiency1Nov 19, 2024
Amyloidosis, hereditary systemic 13Nov 19, 2024
Amyotrophic lateral sclerosis type 13Nov 19, 2024
Amyotrophic lateral sclerosis type 121Nov 19, 2024
Amyotrophic lateral sclerosis type 152Jul 18, 2024
Amyotrophic lateral sclerosis type 162Jul 18, 2024
Amyotrophic lateral sclerosis type 182Jul 18, 2024
Amyotrophic lateral sclerosis type 2, juvenile1Dec 21, 2022
Amyotrophic lateral sclerosis type 42Nov 19, 2024
Andersen Tawil syndrome3Jul 18, 2024
Androgen resistance syndrome11Nov 19, 2024
Anemia, congenital dyserythropoietic, type 1a2Dec 21, 2022
Anemia, nonspherocytic hemolytic, due to G6PD deficiency14Nov 19, 2024
Aneurysm-osteoarthritis syndrome10Nov 19, 2024
Angelman syndrome4Nov 19, 2024
Aniridia 12Jul 18, 2024
Anterior segment dysgenesis2Dec 21, 2022
Anterior segment dysgenesis 11Nov 19, 2024
Anterior segment dysgenesis 31Jul 18, 2024
Aortic aneurysm, familial thoracic 101Jul 18, 2024
Aortic aneurysm, familial thoracic 125Nov 19, 2024
Aortic aneurysm, familial thoracic 414Nov 19, 2024
Aortic aneurysm, familial thoracic 66Nov 19, 2024
Aortic aneurysm, familial thoracic 75Nov 19, 2024
Aortic aneurysm, familial thoracic 81Jul 18, 2024
Aortic aneurysm, familial thoracic 91Jul 18, 2024
Aortic valve disease 12Nov 19, 2024
Aortic valve disease 21Dec 21, 2022
Aortic valve disease 32Dec 21, 2022
Argininosuccinate lyase deficiency1Jul 18, 2024
Aromatase deficiency1Nov 19, 2024
Arrhinia with choanal atresia and microphthalmia syndrome1Nov 19, 2024
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma1Nov 19, 2024
Arrhythmogenic right ventricular cardiomyopathy4Nov 19, 2024
Arrhythmogenic right ventricular dysplasia 1015Nov 19, 2024
Arrhythmogenic right ventricular dysplasia 113Nov 19, 2024
Arrhythmogenic right ventricular dysplasia 125Nov 19, 2024
Arrhythmogenic right ventricular dysplasia 132Dec 21, 2022
Arrhythmogenic right ventricular dysplasia 513Jul 18, 2024
Arrhythmogenic right ventricular dysplasia 824Nov 19, 2024
Arrhythmogenic right ventricular dysplasia 918Nov 19, 2024
Arterial calcification, generalized, of infancy, 12Oct 1, 2019
Arterial calcification, generalized, of infancy, 24Nov 19, 2024
Arterial tortuosity syndrome3Nov 19, 2024
Arthrogryposis multiplex congenita 62Nov 19, 2024
Arthrogryposis syndrome1Nov 19, 2024
Arthrogryposis, distal, with impaired proprioception and touch9Nov 19, 2024
Arthrogryposis, renal dysfunction, and cholestasis 22Nov 19, 2024
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome1Nov 19, 2024
Arts syndrome1Nov 19, 2024
Asphyxiating thoracic dystrophy 311Nov 19, 2024
Asphyxiating thoracic dystrophy 42Nov 19, 2024
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome5Jul 18, 2024
Ataxia, intention tremor, and hypotonia syndrome, childhood-onset1Nov 19, 2024
Ataxia-pancytopenia syndrome2Nov 19, 2024
Ataxia-telangiectasia syndrome12Nov 19, 2024
Atrial conduction disease3Jul 18, 2024
Atrial fibrillation, familial, 131Nov 19, 2024
Atrial fibrillation, familial, 61Nov 19, 2024
Atrial fibrillation, familial, 71Dec 21, 2022
Atrial septal defect 21Jul 18, 2024
Atrial septal defect 38Jul 18, 2024
Atrial septal defect 41Jul 18, 2024
Atrial septal defect 62Dec 21, 2022
Atrial septal defect 72Jul 18, 2024
Atrial septal defect 81Dec 21, 2022
Atrial septal defect 91Dec 21, 2022
Atrioventricular block1Nov 19, 2024
Atrioventricular septal defect 51Dec 21, 2022
Atrophia bulborum hereditaria3Nov 19, 2024
Atypical glycine encephalopathy2Nov 19, 2024
Atypical hemolytic-uremic syndrome with C3 anomaly1Nov 19, 2024
Atypical hemolytic-uremic syndrome with I factor anomaly2Apr 4, 2023
Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1Nov 19, 2024
Au-Kline syndrome6Nov 19, 2024
Auditory neuropathy-optic atrophy syndrome3Jul 18, 2024
Autism1Nov 19, 2024
Autism spectrum disorder3Nov 19, 2024
Autism spectrum disorder due to AUTS2 deficiency5Jul 18, 2024
Autism, susceptibility to, 173Jul 18, 2024
Autism, susceptibility to, 52Nov 19, 2024
Autism, susceptibility to, X-linked 23Nov 19, 2024
Autism, susceptibility to, X-linked 41Nov 19, 2024
Autoimmune lymphoproliferative syndrome1Nov 19, 2024
Autoinflammation with arthritis and dyskeratosis1Nov 19, 2024
Autosomal dominant Alport syndrome2Nov 19, 2024
Autosomal dominant Charcot-Marie-Tooth disease type 2W1Nov 19, 2024
Autosomal dominant Kenny-Caffey syndrome4Nov 19, 2024
Autosomal dominant Parkinson disease 42Nov 19, 2024
Autosomal dominant Parkinson disease 82Jul 18, 2024
Autosomal dominant Robinow syndrome 23Jul 18, 2024
Autosomal dominant Robinow syndrome 31Nov 19, 2024
Autosomal dominant centronuclear myopathy1Nov 19, 2024
Autosomal dominant cerebellar ataxia, deafness and narcolepsy1Jul 18, 2024
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures2Nov 19, 2024
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures2Jul 18, 2024
Autosomal dominant deafness - onychodystrophy syndrome1Dec 21, 2022
Autosomal dominant distal renal tubular acidosis1Nov 19, 2024
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome4Jul 18, 2024
Autosomal dominant hypocalcemia 12Nov 19, 2024
Autosomal dominant ichthyosis vulgaris5Nov 19, 2024
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome14Nov 19, 2024
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome1Nov 19, 2024
Autosomal dominant limb-girdle muscular dystrophy type 1F1Dec 21, 2022
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia1Dec 21, 2022
Autosomal dominant nocturnal frontal lobe epilepsy 11Jul 18, 2024
Autosomal dominant nonsyndromic hearing loss 12Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 102Jul 18, 2024
Autosomal dominant nonsyndromic hearing loss 114Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 128Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 133Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 152Dec 21, 2022
Autosomal dominant nonsyndromic hearing loss 171Jul 18, 2024
Autosomal dominant nonsyndromic hearing loss 202Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 223Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 281Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 2A6Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 3A2Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 401Dec 21, 2022
Autosomal dominant nonsyndromic hearing loss 441Dec 21, 2022
Autosomal dominant nonsyndromic hearing loss 4A1Dec 21, 2022
Autosomal dominant nonsyndromic hearing loss 561Dec 21, 2022
Autosomal dominant nonsyndromic hearing loss 62Nov 19, 2024
Autosomal dominant nonsyndromic hearing loss 72Jul 18, 2024
Autosomal dominant nonsyndromic hearing loss 91Nov 19, 2024
Autosomal dominant omodysplasia1Dec 21, 2022
Autosomal dominant optic atrophy classic form7Nov 19, 2024
Autosomal dominant osteopetrosis 11Nov 19, 2024
Autosomal dominant pseudohypoaldosteronism type 11Jul 18, 2024
Autosomal dominant sensory ataxia 11Nov 19, 2024
Autosomal dominant spastic paraplegia type 91Nov 19, 2024
Autosomal dominant vitreoretinochoroidopathy1Nov 19, 2024
Autosomal recessive Alport syndrome7Nov 19, 2024
Autosomal recessive DOPA responsive dystonia2Jul 18, 2024
Autosomal recessive ataxia due to ubiquinone deficiency1Nov 19, 2024
Autosomal recessive ataxia, Beauce type10Nov 19, 2024
Autosomal recessive bestrophinopathy2Nov 19, 2024
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome6Nov 19, 2024
Autosomal recessive complex spastic paraplegia type 9B1Nov 19, 2024
Autosomal recessive congenital ichthyosis 13Jul 18, 2024
Autosomal recessive congenital ichthyosis 32Jul 18, 2024
Autosomal recessive congenital ichthyosis 4A2Jul 18, 2024
Autosomal recessive congenital ichthyosis 4B1Dec 21, 2022
Autosomal recessive congenital ichthyosis 61Dec 21, 2022
Autosomal recessive distal spinal muscular atrophy 13Dec 21, 2022
Autosomal recessive early-onset Parkinson disease 232Dec 21, 2022
Autosomal recessive early-onset Parkinson disease 61Jul 18, 2024
Autosomal recessive hypophosphatemic bone disease6Nov 19, 2024
Autosomal recessive inherited pseudoxanthoma elasticum5Nov 19, 2024
Autosomal recessive juvenile Parkinson disease 23Jul 18, 2024
Autosomal recessive limb-girdle muscular dystrophy1Nov 19, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2A8Nov 19, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2B3Dec 21, 2022
Autosomal recessive limb-girdle muscular dystrophy type 2I3Nov 19, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2L3Nov 19, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2O1Jul 18, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2P1Dec 21, 2022
Autosomal recessive limb-girdle muscular dystrophy type 2U1Dec 21, 2022
Autosomal recessive non-syndromic intellectual disability1Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 124Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 164Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 18A3Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 18B7Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 1A42Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 1B1Apr 4, 2023
Autosomal recessive nonsyndromic hearing loss 211Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 214Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 223Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 251Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 283Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 291Dec 21, 2022
Autosomal recessive nonsyndromic hearing loss 315Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 302Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 351Dec 21, 2022
Autosomal recessive nonsyndromic hearing loss 361Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 371Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 414Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 421Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 491Dec 21, 2022
Autosomal recessive nonsyndromic hearing loss 632Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 671Dec 21, 2022
Autosomal recessive nonsyndromic hearing loss 72Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 775Jul 18, 2024
Autosomal recessive nonsyndromic hearing loss 791Dec 21, 2022
Autosomal recessive nonsyndromic hearing loss 86Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 84A7Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 84B1Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 864Nov 19, 2024
Autosomal recessive nonsyndromic hearing loss 99Nov 19, 2024
Autosomal recessive omodysplasia1Dec 21, 2022
Autosomal recessive osteopetrosis 13Nov 19, 2024
Autosomal recessive osteopetrosis 41Nov 19, 2024
Autosomal recessive osteopetrosis 51Nov 19, 2024
Autosomal recessive polycystic kidney disease10Nov 19, 2024
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency1Dec 21, 2022
Autosomal recessive spastic paraplegia type 761Dec 21, 2022
Autosomal recessive spinocerebellar ataxia 103Dec 21, 2022
Autosomal recessive spinocerebellar ataxia 131Nov 19, 2024
Autosomal recessive spinocerebellar ataxia 163Nov 19, 2024
Autosomal recessive titinopathy5Nov 19, 2024
Axenfeld-Rieger syndrome type 11Apr 4, 2023
Ayme-Gripp syndrome1Dec 21, 2022
BAP1-related tumor predisposition syndrome1Nov 19, 2024
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 201Nov 19, 2024
BRAT1-related neurodevelopmental disorder1Apr 4, 2023
Bamforth-Lazarus syndrome1Nov 19, 2024
Band heterotopia of brain2Dec 21, 2022
Baraitser-Winter syndrome 17Nov 19, 2024
Baraitser-winter syndrome 21Dec 21, 2022
Bardet-Biedl syndrome 12Nov 19, 2024
Bardet-Biedl syndrome 103Dec 21, 2022
Bardet-Biedl syndrome 161Jul 18, 2024
Bardet-Biedl syndrome 24Jul 18, 2024
Bardet-Biedl syndrome 31Dec 21, 2022
Bardet-Biedl syndrome 51Jul 18, 2024
Bardet-Biedl syndrome 72Dec 21, 2022
Bardet-Biedl syndrome 92Dec 21, 2022
Bartter disease type 13Jul 18, 2024
Bartter disease type 25Nov 19, 2024
Bartter disease type 31Dec 21, 2022
Bartter disease type 51Dec 21, 2022
Basal cell nevus syndrome 13Jul 18, 2024
Basal ganglia calcification, idiopathic, 51Dec 21, 2022
Basal ganglia calcification, idiopathic, 7, autosomal recessive3Dec 21, 2022
Basilicata-Akhtar syndrome3Nov 19, 2024
Beck-Fahrner syndrome5Nov 19, 2024
Becker muscular dystrophy2Nov 19, 2024
Benign familial hematuria8Aug 30, 2020
Benign hereditary chorea1Dec 21, 2022
Bent bone dysplasia syndrome 11Dec 21, 2022
Bernard-Soulier syndrome, type A2, autosomal dominant3Nov 19, 2024
Beta-D-mannosidosis2Dec 21, 2022
Beta-thalassemia HBB/LCRB7Nov 19, 2024
Bethlem myopathy1Nov 19, 2024
Bethlem myopathy 1A4Nov 19, 2024
Bethlem myopathy 25Nov 19, 2024
Bietti crystalline corneoretinal dystrophy1Dec 21, 2022
Bifunctional peroxisomal enzyme deficiency7Nov 19, 2024
Bilateral frontoparietal polymicrogyria2Dec 21, 2022
Biotin-responsive basal ganglia disease2Nov 1, 2016
Biotinidase deficiency4Nov 19, 2024
Birk-Barel syndrome2Nov 19, 2024
Birt-Hogg-Dube syndrome1Aug 3, 2022
Birt-Hogg-Dube syndrome 11Nov 19, 2024
Blepharocheilodontic syndrome 11Jul 18, 2024
Blepharocheilodontic syndrome 23Nov 19, 2024
Blepharophimosis - intellectual disability syndrome, SBBYS type9Nov 19, 2024
Blepharophimosis, ptosis, and epicanthus inversus syndrome2Jul 18, 2024
Blepharophimosis-impaired intellectual development syndrome2Nov 19, 2024
Bloom syndrome2Jul 18, 2024
Bohring-Opitz syndrome7Nov 19, 2024
Bone fragility with contractures, arterial rupture, and deafness1Dec 21, 2022
Bone marrow failure syndrome 33Jul 18, 2024
Bone marrow failure syndrome 41Dec 21, 2022
Bone mineral density quantitative trait locus 182Nov 19, 2024
Borjeson-Forssman-Lehmann syndrome3Nov 19, 2024
Bosch-Boonstra-Schaaf optic atrophy syndrome10Nov 19, 2024
Brachydactyly type A11Nov 19, 2024
Brachydactyly type C1Nov 19, 2024
Brachydactyly-elbow wrist dysplasia syndrome1Dec 21, 2022
Brain dopamine-serotonin vesicular transport disease1Nov 19, 2024
Brain malformations with or without urinary tract defects7Nov 19, 2024
Brain small vessel disease 1 with or without ocular anomalies2Jul 18, 2024
Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome2Nov 19, 2024
Branchiooculofacial syndrome2Nov 19, 2024
Branchiootic syndrome 11Jul 18, 2024
Branchiootorenal syndrome 13Nov 19, 2024
Breast-ovarian cancer, familial, susceptibility to, 17Nov 19, 2024
Breast-ovarian cancer, familial, susceptibility to, 26Nov 19, 2024
Breast-ovarian cancer, familial, susceptibility to, 41Dec 21, 2022
Brittle cornea syndrome 13Nov 19, 2024
Brown-Vialetto-van Laere syndrome 12Dec 21, 2022
Brown-Vialetto-van Laere syndrome 23Dec 21, 2022
Bruck syndrome 21Nov 19, 2024
Brugada syndrome1Dec 21, 2022
Brugada syndrome 127Nov 19, 2024
Brugada syndrome 21Dec 21, 2022
Brugada syndrome 42Dec 21, 2022
Brunner syndrome1Nov 19, 2024
Bryant-Li-Bhoj neurodevelopmental syndrome 11Nov 19, 2024
Bryant-Li-Bhoj neurodevelopmental syndrome 21Nov 19, 2024
C1Q deficiency1Dec 21, 2022
CACNA1A-related complex neurodevelopmental disorder5Nov 19, 2024
CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY1Nov 19, 2024
CBL-related disorder4Nov 19, 2024
CCDC115-CDG2Jul 18, 2024
CEBALID syndrome4Jul 18, 2024
CEP290-related ciliopathy8Nov 19, 2024
CHARGE syndrome28Nov 19, 2024
CHIME syndrome2Nov 19, 2024
CK syndrome1Nov 19, 2024
CODAS syndrome1Jul 18, 2024
COG4-congenital disorder of glycosylation1Nov 19, 2024
COG6-congenital disorder of glycosylation1Dec 21, 2022
COG8-congenital disorder of glycosylation2Dec 21, 2022
COL4A1 or COL4A2-related cerebral small vessel disease10Apr 4, 2023
COL4A1-related disorder1Nov 19, 2024
Camptomelic dysplasia2Jul 18, 2024
Capillary malformation-arteriovenous malformation 17Jul 18, 2024
Capillary malformation-arteriovenous malformation 29Nov 19, 2024
Cardiac anomalies - developmental delay - facial dysmorphism syndrome22Nov 19, 2024
Cardiac arrhythmia, ankyrin-B-related2Dec 21, 2022
Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies5Jul 18, 2024
Cardiac valvular dysplasia, X-linked2Nov 19, 2024
Cardiac, facial, and digital anomalies with developmental delay3Jul 18, 2024
Cardiac-urogenital syndrome1Dec 21, 2022
Cardioacrofacial dysplasia 21Dec 21, 2022
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 12Nov 19, 2024
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 23Dec 21, 2022
Cardiofaciocutaneous syndrome 16Jul 18, 2024
Cardiofaciocutaneous syndrome 21Dec 21, 2022
Cardiofaciocutaneous syndrome 31Dec 21, 2022
Cardiomyopathy26Nov 19, 2024
Cardiomyopathy, dilated, 2D1Jul 18, 2024
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis3Nov 19, 2024
Cardiomyopathy, familial hypertrophic 2725Nov 19, 2024
Cardiomyopathy, familial hypertrophic, 2814Nov 19, 2024
Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies1Nov 19, 2024
Cardiomyopathy, familial restrictive, 12Nov 19, 2024
Cardiospondylocarpofacial syndrome1Dec 21, 2022
Carey-Fineman-Ziter syndrome 11Nov 19, 2024
Carnitine palmitoyl transferase II deficiency, myopathic form2Nov 19, 2024
Cataract 1 multiple types1Jul 18, 2024
Cataract 15 multiple types1Dec 21, 2022
Cataract 16 multiple types1Nov 19, 2024
Cataract 20 multiple types1Dec 21, 2022
Cataract 21 multiple types1Jul 18, 2024
Cataract 3 multiple types1Jul 18, 2024
Cataract 301Jul 18, 2024
Cataract 381Dec 21, 2022
Cataract 411Nov 19, 2024
Cataract 481Jul 18, 2024
Cataract 5 multiple types2Nov 19, 2024
Cataract 6 multiple types2Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia1Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia 134Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia 24Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia 36Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia 41Nov 19, 2024
Catecholaminergic polymorphic ventricular tachycardia 54Jul 18, 2024
Catifa syndrome2Jul 18, 2024
Caveolinopathy1Nov 19, 2024
Central core myopathy6Nov 19, 2024
Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease1Jul 18, 2024
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 23Nov 19, 2024
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 41Dec 21, 2022
Cerebellar ataxia-hypogonadism syndrome1Dec 21, 2022
Cerebellar atrophy with seizures and variable developmental delay1Dec 21, 2022
Cerebellar atrophy, visual impairment, and psychomotor retardation;5Nov 19, 2024
Cerebellar dysfunction with variable cognitive and behavioral abnormalities4Nov 19, 2024
Cerebellar-facial-dental syndrome1Dec 21, 2022
Cerebral amyloid angiopathy, APP-related3Jul 18, 2024
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 112Nov 19, 2024
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 21Nov 19, 2024
Cerebral cavernous malformation5Nov 19, 2024
Cerebral cavernous malformation 12Dec 21, 2022
Cerebral cavernous malformation 31Nov 19, 2024
Cerebral folate transport deficiency1Jul 18, 2024
Cerebro-costo-mandibular syndrome1Jul 18, 2024
Cerebrooculofacioskeletal syndrome 33Dec 21, 2022
Cerebroretinal microangiopathy with calcifications and cysts 12Nov 19, 2024
Channelopathy-associated congenital insensitivity to pain, autosomal recessive3Nov 19, 2024
Char syndrome1Dec 21, 2022
Charcot-Marie-Tooth Disease, axonal, type 2GG1Jul 18, 2024
Charcot-Marie-Tooth disease2Nov 19, 2024
Charcot-Marie-Tooth disease X-linked dominant 15Nov 19, 2024
Charcot-Marie-Tooth disease X-linked recessive 41Dec 21, 2022
Charcot-Marie-Tooth disease axonal type 2C1Jul 18, 2024
Charcot-Marie-Tooth disease axonal type 2CC1Dec 21, 2022
Charcot-Marie-Tooth disease axonal type 2F1Jul 18, 2024
Charcot-Marie-Tooth disease axonal type 2L1Dec 21, 2022
Charcot-Marie-Tooth disease axonal type 2N1Nov 19, 2024
Charcot-Marie-Tooth disease axonal type 2O1Jul 18, 2024
Charcot-Marie-Tooth disease axonal type 2T1Nov 19, 2024
Charcot-Marie-Tooth disease axonal type 2U1Nov 19, 2024
Charcot-Marie-Tooth disease axonal type 2X1Dec 21, 2022
Charcot-Marie-Tooth disease axonal type 2Z1Jul 18, 2024
Charcot-Marie-Tooth disease dominant intermediate B2Nov 19, 2024
Charcot-Marie-Tooth disease dominant intermediate D1Nov 19, 2024
Charcot-Marie-Tooth disease dominant intermediate E1Dec 21, 2022
Charcot-Marie-Tooth disease dominant intermediate F1Dec 21, 2022
Charcot-Marie-Tooth disease type 1B1Nov 19, 2024
Charcot-Marie-Tooth disease type 1D2Nov 19, 2024
Charcot-Marie-Tooth disease type 1F2Nov 19, 2024
Charcot-Marie-Tooth disease type 2A24Nov 19, 2024
Charcot-Marie-Tooth disease type 2B12Nov 19, 2024
Charcot-Marie-Tooth disease type 2Y1Dec 21, 2022
Charcot-Marie-Tooth disease type 4A1Nov 19, 2024
Charcot-Marie-Tooth disease type 4B32Jul 18, 2024
Charcot-Marie-Tooth disease type 4C5Nov 19, 2024
Charcot-Marie-Tooth disease type 4F1Nov 19, 2024
Charcot-Marie-Tooth disease, axonal, Type 2HH1Jul 18, 2024
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;1Nov 19, 2024
Charcot-Marie-Tooth disease, demyelinating, IIA 1I1Nov 19, 2024
Charcot-marie-tooth disease, axonal, type 2DD2Jul 18, 2024
Charlevoix-Saguenay spastic ataxia4Jul 18, 2024
Childhood apraxia of speech5Jul 18, 2024
Childhood hypophosphatasia2Nov 19, 2024
Childhood onset GLUT1 deficiency syndrome 22Nov 19, 2024
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder2Nov 19, 2024
Chitayat syndrome1Nov 19, 2024
Cholestanol storage disease2Dec 21, 2022
Cholestasis, intrahepatic, of pregnancy, 31Nov 19, 2024
Cholestasis, progressive familial intrahepatic, 42Nov 19, 2024
Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss2Dec 21, 2022
Cholestatic liver disease2Sep 16, 2020
Cholesteryl ester storage disease2Nov 19, 2024
Chondrodysplasia Blomstrand type1Nov 19, 2024
Chondrodysplasia punctata 2 X-linked dominant2Nov 19, 2024
Chopra-Amiel-Gordon syndrome3Nov 19, 2024
Choroidal dystrophy, central areolar 21Nov 19, 2024
Choroideremia5Nov 19, 2024
Christianson syndrome1Nov 19, 2024
Chromosome 2q32-q33 deletion syndrome6Nov 19, 2024
Chronic intestinal pseudoobstruction1Nov 19, 2024
Chudley-McCullough syndrome2Nov 19, 2024
Chylomicron retention disease1Jul 18, 2024
Ciliary dyskinesia, primary, 371Nov 19, 2024
Ciliary dyskinesia, primary, 402Jul 18, 2024
Ciliary dyskinesia, primary, 411Jul 18, 2024
Ciliopathy1Jul 18, 2024
Citrullinemia type I3Jul 18, 2024
Clark-Baraitser syndrome8Nov 19, 2024
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency10Jul 18, 2024
Classic homocystinuria4Nov 19, 2024
Cleft palate1Nov 19, 2024
Cleidocranial dysostosis2Jul 18, 2024
Cobalamin C disease6Nov 19, 2024
Cobblestone lissencephaly without muscular or ocular involvement1Dec 21, 2022
Cockayne syndrome type 28Nov 19, 2024
Coffin-Lowry syndrome5Nov 19, 2024
Coffin-Siris syndrome 127Nov 19, 2024
Coffin-Siris syndrome 103Nov 19, 2024
Coffin-Siris syndrome 113Nov 19, 2024
Coffin-Siris syndrome 65Jul 18, 2024
Coffin-Siris syndrome 73Nov 19, 2024
Coffin-Siris syndrome 81Nov 19, 2024
Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome3Nov 19, 2024
Cognitive impairment with or without cerebellar ataxia3Nov 19, 2024
Cohen syndrome10Jul 18, 2024
Cohen-Gibson syndrome1Jul 18, 2024
Collagen 6-related myopathy7Nov 19, 2024
Colobomatous microphthalmia-rhizomelic dysplasia syndrome1Nov 19, 2024
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome1Jul 18, 2024
Colorectal cancer, hereditary nonpolyposis, type 21Nov 19, 2024
Combined deficiency of sialidase AND beta galactosidase2Nov 19, 2024
Combined immunodeficiency1Nov 19, 2024
Combined immunodeficiency due to LRBA deficiency1Nov 19, 2024
Combined immunodeficiency due to MALT1 deficiency1Jul 18, 2024
Combined immunodeficiency, X-linked1Jul 18, 2024
Combined oxidative phosphorylation defect type 134Dec 21, 2022
Combined oxidative phosphorylation defect type 172Nov 19, 2024
Combined oxidative phosphorylation defect type 204Jul 18, 2024
Combined oxidative phosphorylation defect type 214Nov 19, 2024
Combined oxidative phosphorylation defect type 233Jul 18, 2024
Combined oxidative phosphorylation defect type 241Jul 18, 2024
Combined oxidative phosphorylation defect type 273Nov 19, 2024
Combined oxidative phosphorylation defect type 71Dec 21, 2022
Combined oxidative phosphorylation defect type 83Jul 18, 2024
Combined oxidative phosphorylation deficiency 321Dec 21, 2022
Combined oxidative phosphorylation deficiency 351Jul 18, 2024
Combined oxidative phosphorylation deficiency 392Jul 18, 2024
Combined oxidative phosphorylation deficiency 401Jul 18, 2024
Combined oxidative phosphorylation deficiency 441Nov 19, 2024
Combined oxidative phosphorylation deficiency 551Nov 19, 2024
Complement component 6 deficiency1Jul 18, 2024
Complement component 7 deficiency1Jul 18, 2024
Complement component 9 deficiency1Nov 19, 2024
Complex cortical dysplasia with other brain malformations 15Nov 19, 2024
Complex cortical dysplasia with other brain malformations 22Jul 18, 2024
Complex cortical dysplasia with other brain malformations 52Nov 19, 2024
Complex cortical dysplasia with other brain malformations 62Jul 18, 2024
Complex cortical dysplasia with other brain malformations 71Jul 18, 2024
Complex neurodevelopmental disorder5Nov 19, 2024
Complex neurodevelopmental disorder with motor features2Nov 19, 2024
Cone dystrophy 31Jul 18, 2024
Cone-rod dystrophy 101Nov 19, 2024
Cone-rod dystrophy 132Dec 21, 2022
Cone-rod dystrophy 201Dec 21, 2022
Cone-rod dystrophy 38Nov 19, 2024
Cone-rod dystrophy 52Jul 18, 2024
Cone-rod dystrophy 71Dec 21, 2022
Cone-rod synaptic disorder, congenital nonprogressive1Dec 21, 2022
Congenital absence of salivary gland1Nov 19, 2024
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency3Jul 18, 2024
Congenital adrenal hypoplasia, X-linked4Nov 19, 2024
Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency1Dec 21, 2022
Congenital afibrinogenemia1Nov 19, 2024
Congenital amegakaryocytic thrombocytopenia 14Nov 19, 2024
Congenital anomalies of kidney and urinary tract 21Nov 19, 2024
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay2Nov 19, 2024
Congenital anomaly of kidney and urinary tract1Dec 21, 2022
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome1Jul 18, 2024
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome3Jul 18, 2024
Congenital cataracts-facial dysmorphism-neuropathy syndrome1Dec 21, 2022
Congenital central hypoventilation1Oct 1, 2019
Congenital cerebellar hypoplasia1Dec 21, 2022
Congenital contractural arachnodactyly17Nov 19, 2024
Congenital contractures of the limbs and face, hypotonia, and developmental delay7Nov 19, 2024
Congenital defect of folate absorption2Jul 18, 2024
Congenital disorder of deglycosylation 13Jul 18, 2024
Congenital disorder of deglycosylation 22Jul 18, 2024
Congenital disorder of glycosylation type 1E1Dec 21, 2022
Congenital disorder of glycosylation, type IAA2Nov 19, 2024
Congenital disorder of glycosylation, type IIr2Nov 19, 2024
Congenital disorder of glycosylation, type Iw, autosomal dominant1Nov 19, 2024
Congenital dyserythropoietic anemia, type II5Nov 19, 2024
Congenital factor V deficiency3Nov 19, 2024
Congenital factor VII deficiency2Jul 18, 2024
Congenital fibrosis of extraocular muscles1Nov 19, 2024
Congenital fibrosis of extraocular muscles type 11Dec 21, 2022
Congenital generalized lipodystrophy type 12Dec 21, 2022
Congenital generalized lipodystrophy type 21Nov 19, 2024
Congenital heart defects and ectodermal dysplasia2Dec 21, 2022
Congenital heart defects and skeletal malformations syndrome1Jul 18, 2024
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder7Jul 18, 2024
Congenital heart defects, multiple types3Nov 19, 2024
Congenital heart defects, multiple types, 24Nov 19, 2024
Congenital heart defects, multiple types, 43Nov 19, 2024
Congenital heart defects, multiple types, 51Nov 19, 2024
Congenital heart defects, multiple types, 62Dec 21, 2022
Congenital heart defects, multiple types, 74Jul 18, 2024
Congenital heart disease2Jul 18, 2024
Congenital hyperammonemia, type I7Nov 19, 2024
Congenital isolated adrenocorticotropic hormone deficiency1Jul 18, 2024
Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type2Nov 19, 2024
Congenital long QT syndrome3Nov 19, 2024
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome1Jul 18, 2024
Congenital microvillous atrophy2Jul 18, 2024
Congenital multicore myopathy with external ophthalmoplegia4Nov 19, 2024
Congenital muscular hypertrophy-cerebral syndrome6Nov 19, 2024
Congenital myasthenic syndrome 101Dec 21, 2022
Congenital myasthenic syndrome 113Jul 18, 2024
Congenital myasthenic syndrome 192Nov 19, 2024
Congenital myasthenic syndrome 2C1Nov 19, 2024
Congenital myasthenic syndrome 4A1Nov 19, 2024
Congenital myasthenic syndrome 54Nov 19, 2024
Congenital myasthenic syndrome 81Jul 18, 2024
Congenital myopathy3Nov 19, 2024
Congenital myotonia, autosomal recessive form5Nov 19, 2024
Congenital nongoitrous hypothyroidism 62Nov 19, 2024
Congenital nonprogressive myopathy with Moebius and Robin sequences1Dec 21, 2022
Congenital ocular coloboma1Nov 19, 2024
Congenital primary aphakia1Nov 19, 2024
Congenital secretory sodium diarrhea 31Jul 18, 2024
Congenital stationary night blindness 1E1Dec 21, 2022
Congenital stationary night blindness 1F1Jul 18, 2024
Congenital stationary night blindness 2A1Nov 19, 2024
Connective tissue disorder1Nov 19, 2024
Cornelia de Lange syndrome 123Nov 19, 2024
Cornelia de Lange syndrome 31Dec 21, 2022
Cornelia de Lange syndrome 42Nov 19, 2024
Cornelia de Lange syndrome 52Aug 30, 2020
Cortical dysplasia, complex, with other brain malformations 104Nov 19, 2024
Cortical dysplasia, complex, with other brain malformations 91Dec 21, 2022
Cortical dysplasia-focal epilepsy syndrome2Jul 18, 2024
Costello syndrome5Jul 18, 2024
Cowden syndrome 18Nov 19, 2024
Cowden syndrome 51Dec 21, 2022
Cowden syndrome 61Dec 21, 2022
Coxopodopatellar syndrome1Nov 19, 2024
Cranioectodermal dysplasia 12Nov 19, 2024
Craniofacial microsomia 11Jul 18, 2024
Craniofrontonasal syndrome3Nov 19, 2024
Craniosynostosis 21Jul 18, 2024
Craniosynostosis 43Nov 19, 2024
Craniosynostosis 72Jul 18, 2024
Craniosynostosis and dental anomalies1Nov 19, 2024
Craniosynostosis syndrome2Nov 19, 2024
Craniosynostosis with ectopia lentis2Jul 18, 2024
Creatine transporter deficiency3Nov 19, 2024
Crouzon syndrome2Nov 19, 2024
Crouzon syndrome-acanthosis nigricans syndrome1Nov 19, 2024
Cryopyrin associated periodic syndrome1Dec 21, 2022
Cryptorchidism1Dec 21, 2022
Currarino triad3Jul 18, 2024
Curry-Hall syndrome1Nov 19, 2024
Cutaneous photosensitivity2Sep 16, 2020
Cutaneous porphyria2Nov 19, 2024
Cutis laxa with osteodystrophy1Jul 18, 2024
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies1Dec 21, 2022
Cutis laxa, autosomal dominant 12Dec 21, 2022
Cutis laxa, autosomal dominant 31Nov 19, 2024
Cutis laxa, autosomal recessive, type 1B2Jul 18, 2024
Cyclical neutropenia1Nov 19, 2024
Cystic fibrosis2Apr 4, 2023
Cystinuria12Nov 19, 2024
D-2-hydroxyglutaric aciduria 12Dec 21, 2022
D-2-hydroxyglutaric aciduria 21Dec 21, 2022
DDX41-related hematologic malignancy predisposition syndrome1Nov 19, 2024
DEGCAGS syndrome1Jul 18, 2024
DYRK1A-related intellectual disability syndrome9Jul 18, 2024
Danon disease3Nov 19, 2024
De Lange syndrome2Jul 18, 2024
DeSanto-Shinawi syndrome1Jul 18, 2024
DeSanto-Shinawi syndrome due to WAC point mutation1Nov 19, 2024
Deafness with labyrinthine aplasia, microtia, and microdontia3Nov 19, 2024
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome3Nov 19, 2024
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase2Jul 18, 2024
Deficiency of acetyl-CoA acetyltransferase1Dec 21, 2022
Deficiency of adenosine deaminase 21Nov 19, 2024
Deficiency of alpha-mannosidase2Jul 18, 2024
Deficiency of aromatic-L-amino-acid decarboxylase4Dec 21, 2022
Deficiency of beta-ureidopropionase1Nov 19, 2024
Deficiency of butyryl-CoA dehydrogenase2Dec 21, 2022
Deficiency of butyrylcholinesterase4Nov 19, 2024
Deficiency of ferroxidase1Nov 19, 2024
Deficiency of guanidinoacetate methyltransferase2Jul 18, 2024
Deficiency of hydroxymethylglutaryl-CoA lyase2Nov 19, 2024
Deficiency of iodide peroxidase1Dec 21, 2022
Deficiency of malonyl-CoA decarboxylase3Jul 18, 2024
Deficiency of steroid 11-beta-monooxygenase2Nov 19, 2024
Deficiency of steroid 17-alpha-monooxygenase1Nov 19, 2024
Delayed sleep phase syndrome, susceptibility to1Jul 18, 2024
Dent disease type 111Nov 19, 2024
Dent disease type 21Jul 18, 2024
Dentinogenesis imperfecta1Nov 19, 2024
Dermatofibrosis lenticularis disseminata1Nov 19, 2024
Desbuquois dysplasia 11Jul 18, 2024
Desmin-related myofibrillar myopathy2Nov 19, 2024
Developmental and epileptic encephalopathy 1001Nov 19, 2024
Developmental and epileptic encephalopathy 1033Nov 19, 2024
Developmental and epileptic encephalopathy 1061Nov 19, 2024
Developmental and epileptic encephalopathy 1082Jul 18, 2024
Developmental and epileptic encephalopathy 1121Nov 19, 2024
Developmental and epileptic encephalopathy 6B1Jul 18, 2024
Developmental and epileptic encephalopathy 911Dec 21, 2022
Developmental and epileptic encephalopathy 923Jul 18, 2024
Developmental and epileptic encephalopathy 934Nov 19, 2024
Developmental and epileptic encephalopathy 9411Jul 18, 2024
Developmental and epileptic encephalopathy 961Jul 18, 2024
Developmental and epileptic encephalopathy 971Nov 19, 2024
Developmental and epileptic encephalopathy 981Nov 19, 2024
Developmental and epileptic encephalopathy, 1115Nov 19, 2024
Developmental and epileptic encephalopathy, 121Jul 18, 2024
Developmental and epileptic encephalopathy, 1310Nov 19, 2024
Developmental and epileptic encephalopathy, 148Nov 19, 2024
Developmental and epileptic encephalopathy, 162Jul 18, 2024
Developmental and epileptic encephalopathy, 173Jul 18, 2024
Developmental and epileptic encephalopathy, 187Jul 18, 2024
Developmental and epileptic encephalopathy, 28Nov 19, 2024
Developmental and epileptic encephalopathy, 234Jul 18, 2024
Developmental and epileptic encephalopathy, 241Dec 21, 2022
Developmental and epileptic encephalopathy, 266Nov 19, 2024
Developmental and epileptic encephalopathy, 283Jul 18, 2024
Developmental and epileptic encephalopathy, 31A3Nov 19, 2024
Developmental and epileptic encephalopathy, 322Jul 18, 2024
Developmental and epileptic encephalopathy, 331Jul 18, 2024
Developmental and epileptic encephalopathy, 353Jul 18, 2024
Developmental and epileptic encephalopathy, 362Nov 19, 2024
Developmental and epileptic encephalopathy, 391Dec 21, 2022
Developmental and epileptic encephalopathy, 416Nov 19, 2024
Developmental and epileptic encephalopathy, 4211Nov 19, 2024
Developmental and epileptic encephalopathy, 434Jul 18, 2024
Developmental and epileptic encephalopathy, 444Nov 19, 2024
Developmental and epileptic encephalopathy, 451Dec 21, 2022
Developmental and epileptic encephalopathy, 461Jul 18, 2024
Developmental and epileptic encephalopathy, 481Nov 19, 2024
Developmental and epileptic encephalopathy, 55Jul 18, 2024
Developmental and epileptic encephalopathy, 508Nov 19, 2024
Developmental and epileptic encephalopathy, 522Nov 19, 2024
Developmental and epileptic encephalopathy, 544Nov 19, 2024
Developmental and epileptic encephalopathy, 561Jul 18, 2024
Developmental and epileptic encephalopathy, 573Jul 18, 2024
Developmental and epileptic encephalopathy, 581Dec 21, 2022
Developmental and epileptic encephalopathy, 65Nov 19, 2024
Developmental and epileptic encephalopathy, 601Dec 21, 2022
Developmental and epileptic encephalopathy, 624Nov 19, 2024
Developmental and epileptic encephalopathy, 643Jul 18, 2024
Developmental and epileptic encephalopathy, 651Nov 19, 2024
Developmental and epileptic encephalopathy, 663Nov 19, 2024
Developmental and epileptic encephalopathy, 673Jul 18, 2024
Developmental and epileptic encephalopathy, 697Nov 19, 2024
Developmental and epileptic encephalopathy, 718Nov 19, 2024
Developmental and epileptic encephalopathy, 703Nov 19, 2024
Developmental and epileptic encephalopathy, 711Dec 21, 2022
Developmental and epileptic encephalopathy, 722Dec 21, 2022
Developmental and epileptic encephalopathy, 732Nov 19, 2024
Developmental and epileptic encephalopathy, 742Jul 18, 2024
Developmental and epileptic encephalopathy, 754Jul 18, 2024
Developmental and epileptic encephalopathy, 761Nov 19, 2024
Developmental and epileptic encephalopathy, 783Nov 19, 2024
Developmental and epileptic encephalopathy, 791Jul 18, 2024
Developmental and epileptic encephalopathy, 831Jul 18, 2024
Developmental and epileptic encephalopathy, 842Nov 19, 2024
Developmental and epileptic encephalopathy, 85, with or without midline brain defects1Jul 18, 2024
Developmental and epileptic encephalopathy, 871Dec 21, 2022
Developmental and epileptic encephalopathy, 98Nov 19, 2024
Developmental delay and seizures with or without movement abnormalities1Nov 19, 2024
Developmental delay with autism spectrum disorder and gait instability8Nov 19, 2024
Developmental delay with dysmorphic facies and dental anomalies1Jul 18, 2024
Developmental delay with or without dysmorphic facies and autism16Nov 19, 2024
Developmental delay with or without intellectual impairment or behavioral abnormalities2Nov 19, 2024
Developmental delay with variable intellectual impairment and behavioral abnormalities7Nov 19, 2024
Developmental delay with variable neurologic and brain abnormalities2Jul 18, 2024
Developmental delay, behavioral abnormalities, and neuropsychiatric disorders1Jul 18, 2024
Developmental delay, dysmorphic facies, and brain anomalies1Nov 19, 2024
Developmental delay, hypotonia, and impaired language2Nov 19, 2024
Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities1Nov 19, 2024
Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy2Nov 19, 2024
Developmental delay, impaired speech, and behavioral abnormalities7Nov 19, 2024
Developmental delay, impaired speech, and behavioral abnormalities, with or without seizures3Nov 19, 2024
Developmental malformations-deafness-dystonia syndrome2Dec 21, 2022
DiGeorge syndrome1Jul 18, 2024
Diabetes insipidus, nephrogenic, X-linked4Nov 19, 2024
Diabetes insipidus, nephrogenic, autosomal1Nov 19, 2024
Diamond-Blackfan anemia 12Nov 19, 2024
Diamond-Blackfan anemia 102Nov 19, 2024
Diamond-Blackfan anemia 122Nov 19, 2024
Diamond-Blackfan anemia 64Jul 18, 2024
Diamond-Blackfan anemia 81Nov 19, 2024
Diaphyseal dysplasia1Jul 18, 2024
Dias-Logan syndrome4Nov 19, 2024
Diencephalic-mesencephalic junction dysplasia syndrome 13Jul 18, 2024
Diets-Jongmans syndrome1Jul 18, 2024
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome2Dec 21, 2022
Diffuse nonepidermolytic palmoplantar keratoderma2Dec 21, 2022
Dihydropyrimidinase deficiency2Nov 19, 2024
Dihydropyrimidine dehydrogenase deficiency8Dec 21, 2022
Dilated cardiomyopathy 1A17Nov 19, 2024
Dilated cardiomyopathy 1AA7Nov 19, 2024
Dilated cardiomyopathy 1BB6Nov 19, 2024
Dilated cardiomyopathy 1C3Dec 21, 2022
Dilated cardiomyopathy 1CC4Nov 19, 2024
Dilated cardiomyopathy 1D11Nov 19, 2024
Dilated cardiomyopathy 1DD11Jul 18, 2024
Dilated cardiomyopathy 1E9Nov 19, 2024
Dilated cardiomyopathy 1EE1Dec 21, 2022
Dilated cardiomyopathy 1FF3Nov 19, 2024
Dilated cardiomyopathy 1G74Nov 19, 2024
Dilated cardiomyopathy 1HH7Nov 19, 2024
Dilated cardiomyopathy 1I3Nov 19, 2024
Dilated cardiomyopathy 1JJ3Dec 21, 2022
Dilated cardiomyopathy 1NN2Dec 21, 2022
Dilated cardiomyopathy 1O4Nov 19, 2024
Dilated cardiomyopathy 1P1Jul 18, 2024
Dilated cardiomyopathy 1R1Dec 21, 2022
Dilated cardiomyopathy 1S23Nov 19, 2024
Dilated cardiomyopathy 1W6Jul 18, 2024
Dilated cardiomyopathy 1Y3Nov 19, 2024
Dilated cardiomyopathy 2A2Nov 19, 2024
Dilated cardiomyopathy 3B4Nov 19, 2024
Distal arthrogryposis type 2B11Dec 21, 2022
Distal arthrogryposis type 5D5Jul 18, 2024
Distal myopathy with posterior leg and anterior hand involvement2Jul 18, 2024
Distal spinal muscular atrophy1Dec 21, 2022
Distichiasis-lymphedema syndrome1Dec 21, 2022
Dominant dystrophic epidermolysis bullosa with absence of skin1Nov 19, 2024
Dopa-responsive dystonia due to sepiapterin reductase deficiency3Nov 19, 2024
Drash syndrome1Jul 18, 2024
Duane-radial ray syndrome2Jul 18, 2024
Duchenne and Becker muscular dystrophy3Dec 21, 2022
Duchenne muscular dystrophy12Nov 19, 2024
Dworschak-Punetha neurodevelopmental syndrome2Nov 19, 2024
Dyschromatosis universalis hereditaria 31Nov 19, 2024
Dysequilibrium syndrome1Jul 18, 2024
Dyskeratosis congenita2Nov 19, 2024
Dyskeratosis congenita, X-linked5Nov 19, 2024
Dyskeratosis congenita, autosomal dominant 22Nov 19, 2024
Dyskeratosis congenita, autosomal dominant 32Jul 18, 2024
Dyskeratosis congenita, autosomal recessive 56Nov 19, 2024
Dyskinesia with orofacial involvement, autosomal dominant3Nov 19, 2024
Dystonia 241Jul 18, 2024
Dystonia 251Dec 21, 2022
Dystonia 272Nov 19, 2024
Dystonia 28, childhood-onset2Dec 21, 2022
Dystonia 35, childhood-onset1Jul 18, 2024
Dystonia 53Nov 19, 2024
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities1Nov 19, 2024
Dystonic disorder1Dec 21, 2022
Early infantile epileptic encephalopathy with suppression bursts5Nov 19, 2024
Early-onset myopathy with fatal cardiomyopathy3Nov 19, 2024
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome8Jul 18, 2024
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome4Jul 18, 2024
Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant1Nov 19, 2024
Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis3Nov 19, 2024
Ectodermal dysplasia 4, hair/nail type1Nov 19, 2024
Ectodermal dysplasia and immunodeficiency 12Jul 18, 2024
Ectopia lentis 1, isolated, autosomal dominant1Nov 19, 2024
Ectopia lentis 2, isolated, autosomal recessive2Nov 19, 2024
Ectrodactyly1Aug 15, 2019
Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 31Jul 18, 2024
Ehlers-Danlos syndrome due to tenascin-X deficiency6Nov 19, 2024
Ehlers-Danlos syndrome, arthrochalasia type1Jul 18, 2024
Ehlers-Danlos syndrome, cardiac valvular type1Nov 19, 2024
Ehlers-Danlos syndrome, classic type, 110Nov 19, 2024
Ehlers-Danlos syndrome, classic type, 26Nov 19, 2024
Ehlers-Danlos syndrome, dermatosparaxis type1Dec 21, 2022
Ehlers-Danlos syndrome, dominant type 43Nov 19, 2024
Ehlers-Danlos syndrome, periodontal type 12Nov 19, 2024
Ehlers-Danlos syndrome, spondylocheirodysplastic type1Jul 18, 2024
Ehlers-Danlos syndrome, spondylodysplastic type, 11Dec 21, 2022
Ehlers-Danlos syndrome, spondylodysplastic type, 22Jul 18, 2024
Ehlers-Danlos syndrome, type 49Nov 19, 2024
Ehlers-danlos syndrome, arthrochalasia type, 21Nov 19, 2024
Elliptocytosis 31Aug 15, 2019
Ellis-van Creveld syndrome2Nov 19, 2024
Elsahy-Waters syndrome2Nov 19, 2024
Emery-Dreifuss muscular dystrophy 1, X-linked1Jul 18, 2024
Emery-Dreifuss muscular dystrophy 2, autosomal dominant2Nov 19, 2024
Emery-Dreifuss muscular dystrophy 4, autosomal dominant3Nov 19, 2024
Emery-Dreifuss muscular dystrophy 5, autosomal dominant1Dec 21, 2022
Encephalitis, acute, infection (viral)-induced, susceptibility to, 112Nov 19, 2024
Encephalopathy due to GLUT1 deficiency2Nov 19, 2024
Encephalopathy, acute, infection-induced, susceptibility to, 92Jul 18, 2024
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 13Nov 19, 2024
Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis1Nov 19, 2024
Encephalopathy, progressive, with amyotrophy and optic atrophy1Dec 21, 2022
Enhanced S-cone syndrome1Nov 19, 2024
Epidermolysis bullosa simplex 1A, generalized severe1Nov 19, 2024
Epidermolysis bullosa simplex 2B, generalized intermediate2Nov 19, 2024
Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive1Dec 21, 2022
Epidermolysis bullosa simplex with mottled pigmentation1Nov 19, 2024
Epidermolysis bullosa simplex, Ogna type1Nov 19, 2024
Epidermolysis bullosa, junctional 3B, severe1Jul 18, 2024
Epidermolytic hyperkeratosis 13Nov 19, 2024
Epidermolytic hyperkeratosis 2A, autosomal dominant1Nov 19, 2024
Epilepsy2Nov 19, 2024
Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features1Nov 19, 2024
Epilepsy, childhood absence, susceptibility to, 62Jul 18, 2024
Epilepsy, early-onset, vitamin B6-dependent4Jul 18, 2024
Epilepsy, familial focal, with variable foci 112Nov 19, 2024
Epilepsy, familial focal, with variable foci 21Jul 18, 2024
Epilepsy, familial focal, with variable foci 35Nov 19, 2024
Epilepsy, idiopathic generalized, susceptibility to, 103Nov 19, 2024
Epilepsy, idiopathic generalized, susceptibility to, 151Jul 18, 2024
Epilepsy, progressive myoclonic, 111Jul 18, 2024
Epilepsy, progressive myoclonic, 1B1Nov 19, 2024
Epiphyseal dysplasia, multiple, 33Nov 19, 2024
Episodic ataxia type 12Nov 19, 2024
Episodic ataxia type 26Jul 18, 2024
Episodic ataxia type 61Dec 21, 2022
Episodic kinesigenic dyskinesia 12Jul 18, 2024
Erythrocytosis, familial, 42Jul 18, 2024
Ethylmalonic encephalopathy3Jul 18, 2024
Exostoses, multiple, type 12Nov 19, 2024
Exostoses, multiple, type 22Nov 19, 2024
Exudative vitreoretinopathy 12Jul 18, 2024
Exudative vitreoretinopathy 41Nov 19, 2024
Exudative vitreoretinopathy 51Jul 18, 2024
Exudative vitreoretinopathy 71Dec 21, 2022
FG syndrome 23Nov 19, 2024
FG syndrome 45Nov 19, 2024
FGFR3-related chondrodysplasia2Nov 19, 2024
FRAXE3Nov 19, 2024
Fabry disease6Nov 19, 2024
Facial dysmorphism-immunodeficiency-livedo-short stature syndrome1Dec 21, 2022
Factor H deficiency1Nov 19, 2024
Factor XIII, b subunit, deficiency of1Jul 18, 2024
Failure to thrive2Sep 16, 2020
Familial Alzheimer disease1Jul 18, 2024
Familial Mediterranean fever2Nov 19, 2024
Familial Mediterranean fever, autosomal dominant2Nov 19, 2024
Familial X-linked hypophosphatemic vitamin D refractory rickets5Nov 19, 2024
Familial acute necrotizing encephalopathy2Jul 18, 2024
Familial adenomatous polyposis 14Nov 19, 2024
Familial cancer of breast9Nov 19, 2024
Familial cardiomyopathy2Dec 21, 2022
Familial cystic renal disease2Nov 19, 2024
Familial dysautonomia1Nov 19, 2024
Familial episodic pain syndrome with predominantly lower limb involvement1Dec 21, 2022
Familial hemophagocytic lymphohistiocytosis 23Jul 18, 2024
Familial hemophagocytic lymphohistiocytosis 32Nov 19, 2024
Familial hemophagocytic lymphohistiocytosis 41Dec 21, 2022
Familial hyperkalemic periodic paralysis1Nov 19, 2024
Familial hypobetalipoproteinemia 12Nov 19, 2024
Familial hypocalciuric hypercalcemia 15Nov 19, 2024
Familial hypokalemia-hypomagnesemia27Nov 19, 2024
Familial idiopathic steroid-resistant nephrotic syndrome1Nov 19, 2024
Familial infantile myasthenia2Dec 21, 2022
Familial isolated dilated cardiomyopathy2Dec 21, 2022
Familial juvenile hyperuricemic nephropathy type 110Nov 19, 2024
Familial juvenile hyperuricemic nephropathy type 21Nov 19, 2024
Familial medullary thyroid carcinoma1Dec 21, 2022
Familial meningioma1Jul 18, 2024
Familial ovarian cancer2Nov 19, 2024
Familial partial lipodystrophy, Dunnigan type1Nov 19, 2024
Familial pityriasis rubra pilaris1Dec 21, 2022
Familial renal glucosuria2Nov 19, 2024
Familial temporal lobe epilepsy 73Nov 19, 2024
Familial type 3 hyperlipoproteinemia1Nov 19, 2024
Familial type 5 hyperlipoproteinemia1Nov 19, 2024
Fanconi anemia complementation group A7Nov 19, 2024
Fanconi anemia complementation group B1Jul 18, 2024
Fanconi anemia complementation group C2Jul 18, 2024
Fanconi anemia complementation group D12Nov 19, 2024
Fanconi anemia complementation group D24Nov 19, 2024
Fanconi anemia complementation group G1Dec 21, 2022
Fanconi anemia complementation group J1Nov 19, 2024
Fanconi anemia complementation group L2Nov 19, 2024
Fanconi anemia complementation group N1Nov 19, 2024
Fanconi anemia complementation group O1Jul 18, 2024
Fanconi anemia complementation group P2Dec 21, 2022
Fanconi anemia complementation group Q2Dec 21, 2022
Fanconi anemia complementation group R2Jul 18, 2024
Fanconi anemia, complementation group S2Nov 19, 2024
Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young1Nov 19, 2024
Fanconi renotubular syndrome 51Jul 18, 2024
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 33Jul 18, 2024
Febrile seizures, familial, 81Jul 18, 2024
Feingold syndrome type 13Apr 4, 2023
Fibrochondrogenesis 11Nov 19, 2024
Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement1Jul 18, 2024
Fibrosis of extraocular muscles, congenital, 52Jul 18, 2024
Filippi syndrome2Jul 18, 2024
Finnish congenital nephrotic syndrome16Nov 19, 2024
Floating-Harbor syndrome3Jul 18, 2024
Focal dermal hypoplasia1Jul 18, 2024
Focal segmental glomerulosclerosis 14Nov 19, 2024
Focal segmental glomerulosclerosis 22Nov 19, 2024
Focal segmental glomerulosclerosis 59Nov 19, 2024
Focal segmental glomerulosclerosis 71Nov 19, 2024
Focal segmental glomerulosclerosis 82Dec 21, 2022
Focal segmental glomerulosclerosis and neurodevelopmental syndrome2Jul 18, 2024
Fontaine progeroid syndrome1Jul 18, 2024
Fragile X syndrome1Jul 18, 2024
Fraser syndrome 13Nov 19, 2024
Fraser syndrome 21Jul 18, 2024
Frasier syndrome3Nov 19, 2024
Freeman-Sheldon syndrome1Nov 19, 2024
Frontometaphyseal dysplasia 11Nov 19, 2024
Frontotemporal dementia1Jul 18, 2024
Frontotemporal dementia and/or amyotrophic lateral sclerosis 21Nov 19, 2024
Frontotemporal dementia and/or amyotrophic lateral sclerosis 31Nov 19, 2024
Frontotemporal dementia and/or amyotrophic lateral sclerosis 42Jul 18, 2024
Frontotemporal dementia and/or amyotrophic lateral sclerosis 51Dec 21, 2022
Fuhrmann syndrome1Jul 18, 2024
Fumarase deficiency2Nov 19, 2024
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis1Nov 19, 2024
GLUT1 deficiency syndrome2Jul 18, 2024
GM1 gangliosidosis5Jul 18, 2024
GNE myopathy2Nov 19, 2024
GPR143-related foveal hypoplasia1Nov 19, 2024
GRIK2-related neurodevelopmental disorder1Oct 1, 2019
GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder3Nov 19, 2024
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions4Nov 19, 2024
Gabriele de Vries syndrome1Jul 18, 2024
Galactosylceramide beta-galactosidase deficiency6Nov 19, 2024
Galloway-Mowat syndrome 32Jul 18, 2024
Galloway-Mowat syndrome 42Jul 18, 2024
Galloway-Mowat syndrome 62Nov 19, 2024
Gamma-aminobutyric acid transaminase deficiency2Nov 19, 2024
Gastrointestinal defects and immunodeficiency syndrome 16Nov 19, 2024
Gaucher disease3Nov 19, 2024
Gaucher disease perinatal lethal2Jul 18, 2024
Gaucher disease type I5Nov 19, 2024
Gaze palsy, familial horizontal, with progressive scoliosis 13Dec 21, 2022
Geleophysic dysplasia 12Dec 21, 2022
Generalized dominant dystrophic epidermolysis bullosa5Nov 19, 2024
Generalized epilepsy with febrile seizures plus, type 11Nov 19, 2024
Generalized epilepsy with febrile seizures plus, type 101Jul 18, 2024
Generalized epilepsy with febrile seizures plus, type 29Nov 19, 2024
Generalized epilepsy with febrile seizures plus, type 71Nov 19, 2024
Generalized epilepsy-paroxysmal dyskinesia syndrome2Nov 19, 2024
Genitopatellar syndrome1Dec 21, 2022
Genitourinary and/or brain malformation syndrome2Dec 21, 2022
Gillespie syndrome2Nov 19, 2024
Glaucoma 1, open angle, A1Jul 18, 2024
Glaucoma 3A2Jul 18, 2024
Global developmental delay with or without impaired intellectual development4Nov 19, 2024
Global developmental delay with speech and behavioral abnormalities4Nov 19, 2024
Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies2Nov 19, 2024
Global proximal tubulopathy2Sep 16, 2020
Glomerulopathy with fibronectin deposits 27Nov 19, 2024
Glomuvenous malformation2Dec 21, 2022
Glucocorticoid deficiency with achalasia3Nov 19, 2024
Glucose-6-phosphate transport defect2Jul 18, 2024
Glutamate formiminotransferase deficiency1Dec 21, 2022
Glutamate pyruvate transaminase 2 deficiency6Jul 18, 2024
Glutaric aciduria, type 15Jul 18, 2024
Glycine N-methyltransferase deficiency1Jul 18, 2024
Glycine encephalopathy 14Jul 18, 2024
Glycogen storage disease IXa11Nov 19, 2024
Glycogen storage disease IXb1Jul 18, 2024
Glycogen storage disease IXd2Nov 19, 2024
Glycogen storage disease XV1Jul 18, 2024
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form1Jul 18, 2024
Glycogen storage disease due to muscle beta-enolase deficiency2Dec 21, 2022
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency4Nov 19, 2024
Glycogen storage disease type III5Nov 19, 2024
Glycogen storage disease, type II8Nov 19, 2024
Glycogen storage disease, type IV1Nov 19, 2024
Glycogen storage disease, type V4Dec 21, 2022
Glycogen storage disorder due to hepatic glycogen synthase deficiency4Jul 18, 2024
Glycosylphosphatidylinositol biosynthesis defect 152Jul 18, 2024
Glycosylphosphatidylinositol biosynthesis defect 162Nov 19, 2024
Gnathodiaphyseal dysplasia1Nov 19, 2024
Gonadotropin-independent familial sexual precocity1Nov 19, 2024
Gordon syndrome6Nov 19, 2024
Gorlin syndrome5Nov 19, 2024
Grange syndrome1Jul 18, 2024
Granulomatous disease, chronic, X-linked3Nov 19, 2024
Greig cephalopolysyndactyly syndrome3Jul 18, 2024
Growth delay due to insulin-like growth factor I resistance3Nov 19, 2024
Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy3Dec 21, 2022
H syndrome2Jul 18, 2024
HSD10 mitochondrial disease1Oct 1, 2019
HUWE1-related neurodevelopmental disorder1Oct 1, 2019
Hajdu-Cheney syndrome3Jul 18, 2024
Hamartoma of hypothalamus1Dec 21, 2022
Hand-foot-genital syndrome1Dec 21, 2022
Hao-Fountain syndrome1Dec 21, 2022
Hao-Fountain syndrome due to USP7 mutation2Nov 19, 2024
Harel-Yoon syndrome4Nov 19, 2024
Hearing loss, X-linked 61Nov 19, 2024
Hearing loss, autosomal dominant 731Nov 19, 2024
Hearing loss, autosomal dominant 761Jul 18, 2024
Hearing loss, autosomal dominant 781Nov 19, 2024
Hearing loss, autosomal dominant 801Nov 19, 2024
Hearing loss, autosomal recessive1Nov 19, 2024
Hearing loss, autosomal recessive 1001Jul 18, 2024
Hearing loss, autosomal recessive 1103Nov 19, 2024
Hearing loss, autosomal recessive 575Nov 19, 2024
Heart defect - tongue hamartoma - polysyndactyly syndrome2Jul 18, 2024
Hecht syndrome3Jul 18, 2024
Hematuria, benign familial, 11Nov 19, 2024
Hemochromatosis type 13Jul 18, 2024
Hemochromatosis type 2A2Dec 21, 2022
Hemochromatosis type 31Dec 21, 2022
Hemoglobin E disease1Nov 19, 2024
Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature1Nov 19, 2024
Hemolytic uremic syndrome, atypical, susceptibility to, 13Nov 19, 2024
Hemorrhage, intracerebral, susceptibility to1Nov 19, 2024
Hennekam lymphangiectasia-lymphedema syndrome 11Jul 18, 2024
Hepatic veno-occlusive disease-immunodeficiency syndrome1Jul 18, 2024
Hereditary acrodermatitis enteropathica2Jul 18, 2024
Hereditary arterial and articular multiple calcification syndrome1Dec 21, 2022
Hereditary breast ovarian cancer syndrome1Nov 19, 2024
Hereditary cancer-predisposing syndrome3Nov 19, 2024
Hereditary coproporphyria1Nov 19, 2024
Hereditary factor IX deficiency disease1Dec 21, 2022
Hereditary factor VIII deficiency disease10Nov 19, 2024
Hereditary factor XI deficiency disease6Nov 19, 2024
Hereditary fructosuria3Dec 21, 2022
Hereditary insensitivity to pain with anhidrosis1Nov 19, 2024
Hereditary leiomyomatosis and renal cell cancer1Nov 19, 2024
Hereditary lipodystrophy1Nov 19, 2024
Hereditary lymphedema type I3Nov 19, 2024
Hereditary orotic aciduria2Nov 19, 2024
Hereditary sensory and autonomic neuropathy type 61Dec 21, 2022
Hereditary sensory and autonomic neuropathy type 71Nov 19, 2024
Hereditary sensory neuropathy-deafness-dementia syndrome5Nov 19, 2024
Hereditary spastic paraplegia2Nov 19, 2024
Hereditary spastic paraplegia 103Nov 19, 2024
Hereditary spastic paraplegia 1116Nov 19, 2024
Hereditary spastic paraplegia 158Jul 18, 2024
Hereditary spastic paraplegia 21Jul 18, 2024
Hereditary spastic paraplegia 281Jul 18, 2024
Hereditary spastic paraplegia 305Nov 19, 2024
Hereditary spastic paraplegia 311Jul 18, 2024
Hereditary spastic paraplegia 352Dec 21, 2022
Hereditary spastic paraplegia 392Nov 19, 2024
Hereditary spastic paraplegia 3A4Jul 18, 2024
Hereditary spastic paraplegia 417Nov 19, 2024
Hereditary spastic paraplegia 474Nov 19, 2024
Hereditary spastic paraplegia 485Nov 19, 2024
Hereditary spastic paraplegia 492Nov 19, 2024
Hereditary spastic paraplegia 501Jul 18, 2024
Hereditary spastic paraplegia 531Dec 21, 2022
Hereditary spastic paraplegia 541Jul 18, 2024
Hereditary spastic paraplegia 562Jul 18, 2024
Hereditary spastic paraplegia 5A1Dec 21, 2022
Hereditary spastic paraplegia 61Dec 21, 2022
Hereditary spastic paraplegia 76Nov 19, 2024
Hereditary spastic paraplegia 731Jul 18, 2024
Hereditary spastic paraplegia 742Dec 21, 2022
Hereditary spherocytosis type 21Oct 1, 2019
Hereditary spherocytosis type 32Nov 19, 2024
Hereditary spherocytosis type 41Nov 19, 2024
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX12Nov 19, 2024
Hereditary thrombophilia due to congenital protein S deficiency2Nov 19, 2024
Hereditary von Willebrand disease4Nov 19, 2024
Hereditary xanthinuria type 11Jul 18, 2024
Hermansky-Pudlak syndrome 12Nov 19, 2024
Hermansky-Pudlak syndrome 32Nov 19, 2024
Hermansky-Pudlak syndrome 52Nov 19, 2024
Hermansky-Pudlak syndrome 62Jul 18, 2024
Heterotaxy, visceral, 1, X-linked4Nov 19, 2024
Heterotaxy, visceral, 5, autosomal2Nov 19, 2024
Heterotaxy, visceral, 8, autosomal3Nov 19, 2024
Heterotopia, periventricular, X-linked dominant4Nov 19, 2024
Hiatt-Neu-Cooper neurodevelopmental syndrome2Jul 18, 2024
Hidrotic ectodermal dysplasia syndrome2Nov 19, 2024
Hirschsprung disease, susceptibility to, 12Jul 18, 2024
Hirschsprung disease, susceptibility to, 21Nov 19, 2024
Histiocytic medullary reticulosis1Jul 18, 2024
Hogue-Janssens syndrome 15Jul 18, 2024
Holocarboxylase synthetase deficiency2Dec 21, 2022
Holoprosencephaly 112Jul 18, 2024
Holoprosencephaly 35Nov 19, 2024
Holoprosencephaly 41Dec 21, 2022
Holoprosencephaly 52Jul 18, 2024
Holoprosencephaly 91Jul 18, 2024
Holt-Oram syndrome6Nov 19, 2024
Homocystinuria due to methylene tetrahydrofolate reductase deficiency6Jul 18, 2024
Houge-Janssens syndrome 21Jul 18, 2024
Houge-Janssens syndrome 32Jul 18, 2024
Hurler syndrome1Jul 18, 2024
Hydatidiform mole, recurrent, 12Nov 19, 2024
Hydrocephalus, nonsyndromic, autosomal recessive 22Dec 21, 2022
Hydrolethalus syndrome 11Jul 18, 2024
Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome2Dec 21, 2022
Hyper-IgM syndrome type 11Nov 19, 2024
Hyperaldosteronism, familial, type IV1Dec 21, 2022
Hypercalcemia, infantile, 11Jul 18, 2024
Hypercalcemia, infantile, 24Nov 19, 2024
Hypercholesterolemia, autosomal dominant, 31Dec 21, 2022
Hypercholesterolemia, autosomal dominant, type B8Nov 19, 2024
Hypercholesterolemia, familial, 131Nov 19, 2024
Hyperekplexia 12Nov 19, 2024
Hyperekplexia 34Nov 19, 2024
Hyperimmunoglobulin D with periodic fever1Jul 18, 2024
Hyperinsulinemic hypoglycemia, familial, 16Nov 19, 2024
Hyperinsulinemic hypoglycemia, familial, 42Dec 21, 2022
Hyperinsulinism due to glucokinase deficiency1Nov 19, 2024
Hyperlipoproteinemia, type I3Nov 19, 2024
Hyperphosphatasia with intellectual disability syndrome 11Dec 21, 2022
Hyperphosphatasia with intellectual disability syndrome 21Dec 21, 2022
Hyperphosphatasia with intellectual disability syndrome 31Dec 21, 2022
Hyperphosphatasia with intellectual disability syndrome 43Nov 19, 2024
Hyperphosphatasia with intellectual disability syndrome 53Jul 18, 2024
Hypertrichotic osteochondrodysplasia Cantu type5Nov 19, 2024
Hypertrophic cardiomyopathy11Nov 19, 2024
Hypertrophic cardiomyopathy 152Nov 19, 2024
Hypertrophic cardiomyopathy 102Jul 18, 2024
Hypertrophic cardiomyopathy 111Dec 21, 2022
Hypertrophic cardiomyopathy 126Nov 19, 2024
Hypertrophic cardiomyopathy 143Dec 21, 2022
Hypertrophic cardiomyopathy 175Nov 19, 2024
Hypertrophic cardiomyopathy 191Dec 21, 2022
Hypertrophic cardiomyopathy 211Jul 18, 2024
Hypertrophic cardiomyopathy 2633Nov 19, 2024
Hypertrophic cardiomyopathy 35Jul 18, 2024
Hypertrophic cardiomyopathy 487Nov 19, 2024
Hypertrophic cardiomyopathy 61Jul 18, 2024
Hypertrophic cardiomyopathy 710Nov 19, 2024
Hypertrophic cardiomyopathy 81Nov 19, 2024
Hypertrophic cardiomyopathy 94Nov 19, 2024
Hyperuricemic nephropathy, familial juvenile type 42Nov 19, 2024
Hypoalphalipoproteinemia, primary, 11Nov 19, 2024
Hypochondroplasia1Nov 19, 2024
Hypogonadism with anosmia1Dec 21, 2022
Hypogonadotropic hypogonadism 1 with or without anosmia3Nov 19, 2024
Hypogonadotropic hypogonadism 14 with or without anosmia3Nov 19, 2024
Hypogonadotropic hypogonadism 2 with or without anosmia3Nov 19, 2024
Hypogonadotropic hypogonadism 25 with anosmia1Jul 18, 2024
Hypogonadotropic hypogonadism 3 with or without anosmia3Nov 19, 2024
Hypogonadotropic hypogonadism 7 with or without anosmia3Nov 19, 2024
Hypohidrotic X-linked ectodermal dysplasia6Nov 19, 2024
Hypokalemic periodic paralysis, type 22Nov 19, 2024
Hypomagnesemia, seizures, and intellectual disability 11Nov 19, 2024
Hypomyelinating leukodystrophy 111Jul 18, 2024
Hypomyelinating leukodystrophy 122Dec 21, 2022
Hypomyelinating leukodystrophy 62Jul 18, 2024
Hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism1Nov 19, 2024
Hypomyelinating leukodystrophy 93Jul 18, 2024
Hypomyelination with brain stem and spinal cord involvement and leg spasticity3Nov 19, 2024
Hypoparathyroidism, deafness, renal disease syndrome6Jul 18, 2024
Hypophosphatasia3Nov 19, 2024
Hypophosphatemic nephrolithiasis/osteoporosis 12Nov 19, 2024
Hypophosphatemic rickets, autosomal recessive, 11Nov 19, 2024
Hypopituitarism1Jul 18, 2024
Hypoplastic left heart syndrome1Dec 21, 2022
Hypospadias 2, X-linked2Nov 19, 2024
Hypothyroidism due to TSH receptor mutations2Nov 19, 2024
Hypotonia with lactic acidemia and hyperammonemia1Dec 21, 2022
Hypotonia, ataxia, and delayed development syndrome4Nov 19, 2024
Hypotonia, infantile, with psychomotor retardation and characteristic facies 26Jul 18, 2024
Hypotonia, infantile, with psychomotor retardation and characteristic facies 32Jul 18, 2024
Hypotrichosis 141Dec 21, 2022
Hypotrichosis 61Dec 21, 2022
Hypotrichosis 81Jul 18, 2024
Ichthyosis prematurity syndrome2Jul 18, 2024
Ichthyosis vulgaris12Nov 19, 2024
Idiopathic basal ganglia calcification 15Jul 18, 2024
Imerslund-Grasbeck syndrome type 14Jul 18, 2024
Immunodeficiency1Jul 18, 2024
Immunodeficiency 1021Jul 18, 2024
Immunodeficiency 31B1Nov 1, 2016
Immunodeficiency 751Jul 18, 2024
Immunodeficiency 771Jul 18, 2024
Immunodeficiency 78 with autoimmunity and developmental delay1Jul 18, 2024
Immunodeficiency 961Jul 18, 2024
Immunodeficiency, common variable, 124Nov 19, 2024
Immunodeficiency, common variable, 22Nov 19, 2024
Immunodeficiency, developmental delay, and hypohomocysteinemia1Dec 21, 2022
Immunodeficiency-centromeric instability-facial anomalies syndrome 21Dec 21, 2022
Infantile GM1 gangliosidosis5Jul 18, 2024
Infantile cerebellar-retinal degeneration3Nov 19, 2024
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome1Nov 19, 2024
Infantile liver failure syndrome 12Jul 18, 2024
Infantile liver failure syndrome 26Nov 19, 2024
Infantile nephronophthisis2Jul 18, 2024
Infantile neuroaxonal dystrophy3Nov 19, 2024
Infantile-onset ascending hereditary spastic paralysis2Dec 21, 2022
Infantile-onset generalized dyskinesia with orofacial involvement2Nov 19, 2024
Insulin-dependent diabetes mellitus secretory diarrhea syndrome1Dec 21, 2022
Intellectual developmental disorder 60 with seizures1Jul 18, 2024
Intellectual developmental disorder 612Jul 18, 2024
Intellectual developmental disorder 628Nov 19, 2024
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature1Jul 18, 2024
Intellectual developmental disorder with autism and dysmorphic facies1Jul 18, 2024
Intellectual developmental disorder with autism and macrocephaly8Jul 18, 2024
Intellectual developmental disorder with autistic features and language delay, with or without seizures5Nov 19, 2024
Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures2Nov 19, 2024
Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities3Nov 19, 2024
Intellectual developmental disorder with dysmorphic facies and ptosis12Nov 19, 2024
Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold2Jul 18, 2024
Intellectual developmental disorder with hypotonia and behavioral abnormalities3Nov 19, 2024
Intellectual developmental disorder with impaired language and dysmorphic facies3Nov 19, 2024
Intellectual developmental disorder with macrocephaly, seizures, and speech delay1Dec 21, 2022
Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies2Jul 18, 2024
Intellectual developmental disorder with ocular anomalies and distinctive facial features1Nov 19, 2024
Intellectual developmental disorder with seizures and language delay11Nov 19, 2024
Intellectual developmental disorder with severe speech and ambulation defects3Nov 19, 2024
Intellectual developmental disorder with short stature and behavioral abnormalities2Dec 21, 2022
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies3Jul 18, 2024
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities6Nov 19, 2024
Intellectual developmental disorder, X-linked 1121Nov 19, 2024
Intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type1Jul 18, 2024
Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies1Nov 19, 2024
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly2Dec 21, 2022
Intellectual developmental disorder, autosomal dominant 6410Nov 19, 2024
Intellectual developmental disorder, autosomal dominant 664Nov 19, 2024
Intellectual developmental disorder, autosomal dominant 672Jul 18, 2024
Intellectual developmental disorder, autosomal dominant 681Nov 19, 2024
Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities1Nov 19, 2024
Intellectual developmental disorder, autosomal dominant 721Nov 19, 2024
Intellectual developmental disorder, autosomal recessive 671Nov 19, 2024
Intellectual developmental disorder, autosomal recessive 711Jul 18, 2024
Intellectual developmental disorder, autosomal recessive 721Dec 21, 2022
Intellectual developmental disorder, autosomal recessive 745Nov 19, 2024
Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly2Jul 18, 2024
Intellectual developmental disorder, autosomal recessive 771Nov 19, 2024
Intellectual developmental disorder, x-linked, syndromic 371Nov 19, 2024
Intellectual disability1Nov 19, 2024
Intellectual disability and myopathy syndrome1Nov 19, 2024
Intellectual disability, FRA12A type1Dec 21, 2022
Intellectual disability, X-linked 111Nov 19, 2024
Intellectual disability, X-linked 1001Jul 18, 2024
Intellectual disability, X-linked 10211Nov 19, 2024
Intellectual disability, X-linked 1041Jul 18, 2024
Intellectual disability, X-linked 1051Nov 19, 2024
Intellectual disability, X-linked 1062Nov 19, 2024
Intellectual disability, X-linked 1072Nov 19, 2024
Intellectual disability, X-linked 211Jul 18, 2024
Intellectual disability, X-linked 302Nov 19, 2024
Intellectual disability, X-linked 494Nov 19, 2024
Intellectual disability, X-linked 612Nov 19, 2024
Intellectual disability, X-linked 632Jul 18, 2024
Intellectual disability, X-linked 903Nov 19, 2024
Intellectual disability, X-linked 934Nov 19, 2024
Intellectual disability, X-linked 961Nov 19, 2024
Intellectual disability, X-linked 971Jul 18, 2024
Intellectual disability, X-linked 999Nov 19, 2024
Intellectual disability, X-linked 99, syndromic, female-restricted8Nov 19, 2024
Intellectual disability, X-linked syndromic, Turner type16Nov 19, 2024
Intellectual disability, X-linked, syndromic 335Nov 19, 2024
Intellectual disability, X-linked, syndromic, Bain type2Nov 19, 2024
Intellectual disability, X-linked, syndromic, Houge type1Nov 19, 2024
Intellectual disability, X-linked, with or without seizures, arx-related1Nov 19, 2024
Intellectual disability, X-linked, with panhypopituitarism2Nov 19, 2024
Intellectual disability, autosomal dominant1Jul 18, 2024
Intellectual disability, autosomal dominant 14Jul 18, 2024
Intellectual disability, autosomal dominant 111Dec 21, 2022
Intellectual disability, autosomal dominant 138Nov 19, 2024
Intellectual disability, autosomal dominant 147Nov 19, 2024
Intellectual disability, autosomal dominant 153Nov 19, 2024
Intellectual disability, autosomal dominant 164Jul 18, 2024
Intellectual disability, autosomal dominant 204Nov 19, 2024
Intellectual disability, autosomal dominant 226Jul 18, 2024
Intellectual disability, autosomal dominant 244Nov 19, 2024
Intellectual disability, autosomal dominant 272Nov 19, 2024
Intellectual disability, autosomal dominant 295Jul 18, 2024
Intellectual disability, autosomal dominant 301Jul 18, 2024
Intellectual disability, autosomal dominant 341Nov 19, 2024
Intellectual disability, autosomal dominant 385Jul 18, 2024
Intellectual disability, autosomal dominant 3911Nov 19, 2024
Intellectual disability, autosomal dominant 401Jul 18, 2024
Intellectual disability, autosomal dominant 415Nov 19, 2024
Intellectual disability, autosomal dominant 425Nov 19, 2024
Intellectual disability, autosomal dominant 435Nov 19, 2024
Intellectual disability, autosomal dominant 459Nov 19, 2024
Intellectual disability, autosomal dominant 461Jul 18, 2024
Intellectual disability, autosomal dominant 474Jul 18, 2024
Intellectual disability, autosomal dominant 483Nov 19, 2024
Intellectual disability, autosomal dominant 515Nov 19, 2024
Intellectual disability, autosomal dominant 504Nov 19, 2024
Intellectual disability, autosomal dominant 514Nov 19, 2024
Intellectual disability, autosomal dominant 5216Jul 18, 2024
Intellectual disability, autosomal dominant 532Dec 21, 2022
Intellectual disability, autosomal dominant 543Jul 18, 2024
Intellectual disability, autosomal dominant 55, with seizures4Jul 18, 2024
Intellectual disability, autosomal dominant 565Nov 19, 2024
Intellectual disability, autosomal dominant 575Jul 18, 2024
Intellectual disability, autosomal dominant 581Jul 18, 2024
Intellectual disability, autosomal dominant 64Nov 19, 2024
Intellectual disability, autosomal dominant 84Nov 19, 2024
Intellectual disability, autosomal dominant 99Nov 19, 2024
Intellectual disability, autosomal recessive 135Jul 18, 2024
Intellectual disability, autosomal recessive 182Nov 19, 2024
Intellectual disability, autosomal recessive 272Dec 21, 2022
Intellectual disability, autosomal recessive 443Dec 21, 2022
Intellectual disability, autosomal recessive 451Nov 19, 2024
Intellectual disability, autosomal recessive 473Dec 21, 2022
Intellectual disability, autosomal recessive 539Nov 19, 2024
Intellectual disability, autosomal recessive 572Jul 18, 2024
Intellectual disability, autosomal recessive 582Dec 21, 2022
Intellectual disability, autosomal recessive 653Nov 19, 2024
Intellectual disability, autosomal recessive 662Jul 18, 2024
Intellectual disability, autosomal recessive 71Jul 18, 2024
Intellectual disability-epilepsy-extrapyramidal syndrome1Nov 19, 2024
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency18Nov 19, 2024
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome6Nov 19, 2024
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome4Nov 19, 2024
Intellectual disability-hypotonic facies syndrome, X-linked, 12Nov 19, 2024
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome6Nov 19, 2024
Intellectual disability-severe speech delay-mild dysmorphism syndrome17Nov 19, 2024
Intellectual disability-strabismus syndrome1Nov 19, 2024
Interstitial lung disease due to ABCA3 deficiency5Jul 18, 2024
Intestinal hypomagnesemia 13Nov 19, 2024
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency3Nov 19, 2024
Isolated congenital megalocornea1Jul 18, 2024
Isolated lutropin deficiency1Dec 21, 2022
Jackson-Weiss syndrome2Jul 18, 2024
Jawad syndrome1Dec 21, 2022
Jervell and Lange-Nielsen syndrome 11Nov 19, 2024
Jervell and Lange-Nielsen syndrome 21Nov 19, 2024
Johanson-Blizzard syndrome1Dec 21, 2022
Joubert syndrome 12Nov 19, 2024
Joubert syndrome 102Nov 19, 2024
Joubert syndrome 132Dec 21, 2022
Joubert syndrome 142Jul 18, 2024
Joubert syndrome 151Jul 18, 2024
Joubert syndrome 162Nov 19, 2024
Joubert syndrome 1711Nov 19, 2024
Joubert syndrome 183Dec 21, 2022
Joubert syndrome 211Jul 18, 2024
Joubert syndrome 235Nov 19, 2024
Joubert syndrome 252Dec 21, 2022
Joubert syndrome 36Jul 18, 2024
Joubert syndrome 302Dec 21, 2022
Joubert syndrome 322Nov 19, 2024
Joubert syndrome 383Jul 18, 2024
Joubert syndrome 51Jul 18, 2024
Joubert syndrome 62Aug 30, 2020
Joubert syndrome 75Nov 19, 2024
Joubert syndrome 97Nov 19, 2024
Junctional epidermolysis bullosa1Jul 18, 2024
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome3Dec 21, 2022
Juvenile retinoschisis2Dec 21, 2022
KAT6B-related multiple congenital anomalies syndrome1Nov 19, 2024
KBG syndrome34Nov 19, 2024
KCNH1 associated disorder3Nov 19, 2024
KIF1A related neurological disorder5Nov 19, 2024
Kabuki syndrome 138Nov 19, 2024
Kabuki syndrome 211Jul 18, 2024
Kallikrein, decreased urinary activity of1Apr 4, 2023
Kartagener syndrome3Nov 19, 2024
Karyomegalic interstitial nephritis6Nov 19, 2024
Keipert syndrome2Jul 18, 2024
Khan-Khan-Katsanis syndrome1Dec 21, 2022
Kleefstra syndrome 19Nov 19, 2024
Kleefstra syndrome 216Nov 19, 2024
Klippel-Feil syndrome 1, autosomal dominant1Nov 19, 2024
Knobloch syndrome 11Nov 19, 2024
Kohlschutter-Tonz syndrome-like1Dec 21, 2022
Koolen-de Vries syndrome4Jul 18, 2024
Kostmann syndrome1Nov 19, 2024
Kugelberg-Welander disease2Dec 21, 2022
Kury-Isidor syndrome1Nov 19, 2024
L-2-hydroxyglutaric aciduria2Nov 19, 2024
L1 syndrome1Nov 19, 2024
LAMA2-related muscular dystrophy6Nov 19, 2024
LAMA5-related multisystemic syndrome1Nov 19, 2024
LAMB2-related infantile-onset nephrotic syndrome1Nov 19, 2024
Lamb-Shaffer syndrome4Nov 19, 2024
Laminopathy3Nov 19, 2024
Landau-Kleffner syndrome3Dec 21, 2022
Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia1Nov 19, 2024
Large congenital melanocytic nevus1Dec 21, 2022
Larsen syndrome1Nov 19, 2024
Lateral meningocele syndrome1Dec 21, 2022
Laurence-Moon syndrome1Dec 21, 2022
Leber congenital amaurosis 12Nov 19, 2024
Leber congenital amaurosis 102Dec 21, 2022
Leber congenital amaurosis 21Nov 19, 2024
Leber congenital amaurosis 32Dec 21, 2022
Leber congenital amaurosis 61Jul 18, 2024
Leber optic atrophy1Apr 4, 2023
Left ventricular noncompaction2Nov 19, 2024
Left ventricular noncompaction 11Jul 18, 2024
Left ventricular noncompaction 104Nov 19, 2024
Left ventricular noncompaction 71Jul 18, 2024
Left ventricular noncompaction 83Jul 18, 2024
Legius syndrome5Nov 19, 2024
Leigh syndrome3Jul 18, 2024
Lesch-Nyhan syndrome1Dec 21, 2022
Lethal acantholytic epidermolysis bullosa1Nov 19, 2024
Lethal congenital contracture syndrome 114Nov 19, 2024
Lethal congenital contracture syndrome 31Nov 19, 2024
Lethal congenital contracture syndrome 91Jul 18, 2024
Lethal congenital glycogen storage disease of heart1Dec 21, 2022
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome3Nov 19, 2024
Leukodystrophy, hypomyelinating, 152Dec 21, 2022
Leukodystrophy, hypomyelinating, 161Dec 21, 2022
Leukodystrophy, hypomyelinating, 19, transient infantile1Jul 18, 2024
Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy1Jul 18, 2024
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome5Nov 19, 2024
Leukoencephalopathy with mild cerebellar ataxia and white matter edema2Nov 19, 2024
Leukoencephalopathy with vanishing white matter 13Nov 19, 2024
Leukoencephalopathy, diffuse hereditary, with spheroids 12Nov 19, 2024
Leukoencephalopathy, progressive, with ovarian failure2Jul 18, 2024
Leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome5Nov 19, 2024
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome4Jul 18, 2024
Levy-Hollister syndrome3Nov 19, 2024
Lewy body dementia1Nov 19, 2024
Li-Ghorbani-Weisz-Hubshman syndrome1Jul 18, 2024
Liang-Wang syndrome1Nov 19, 2024
Linear skin defects with multiple congenital anomalies 31Jul 18, 2024
Lipoyl transferase 1 deficiency3Nov 19, 2024
Lissencephaly 101Dec 21, 2022
Lissencephaly 42Dec 21, 2022
Lissencephaly 9 with complex brainstem malformation1Jul 18, 2024
Lissencephaly due to LIS1 mutation1Nov 19, 2024
Lissencephaly due to TUBA1A mutation11Nov 19, 2024
Lissencephaly type 1 due to doublecortin gene mutation2Dec 21, 2022
Loeys-Dietz syndrome 110Nov 19, 2024
Loeys-Dietz syndrome 24Nov 19, 2024
Loeys-Dietz syndrome 44Jul 18, 2024
Loeys-Dietz syndrome 62Jul 18, 2024
Long QT syndrome 152Nov 19, 2024
Long QT syndrome 101Dec 21, 2022
Long QT syndrome 111Jul 18, 2024
Long QT syndrome 131Dec 21, 2022
Long QT syndrome 151Dec 21, 2022
Long QT syndrome 162Jul 18, 2024
Long QT syndrome 241Nov 19, 2024
Long QT syndrome 317Nov 19, 2024
Long QT syndrome 51Nov 19, 2024
Long QT syndrome 63Dec 21, 2022
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency4Nov 19, 2024
Long qt syndrome 811Nov 19, 2024
Loricrin keratoderma1Dec 21, 2022
Low phospholipid associated cholelithiasis7Nov 19, 2024
Lowe syndrome3Dec 21, 2022
Lower urinary tract obstruction, congenital1Nov 19, 2024
Luscan-Lumish syndrome11Nov 19, 2024
Lymphatic malformation 41Dec 21, 2022
Lymphatic malformation 66Nov 19, 2024
Lymphatic malformation 72Nov 19, 2024
Lynch syndrome 42Nov 19, 2024
Lynch syndrome 51Jul 18, 2024
Lysosomal acid lipase deficiency1Apr 4, 2023
MASA syndrome2Jul 18, 2024
MED12-related intellectual disability syndrome5Nov 19, 2024
MELAS syndrome1Apr 4, 2023
MIRAGE syndrome4Nov 19, 2024
MOGS-congenital disorder of glycosylation3Nov 19, 2024
MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome1Nov 19, 2024
MYPN-related myopathy1Dec 21, 2022
Macrocephaly, acquired, with impaired intellectual development7Nov 19, 2024
Macrocephaly, dysmorphic facies, and psychomotor retardation4Jul 18, 2024
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin2Nov 19, 2024
Macrocephaly-autism syndrome5Jul 18, 2024
Macrocephaly-developmental delay syndrome3Jul 18, 2024
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome10Nov 19, 2024
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss12Nov 19, 2024
Macular corneal dystrophy1Jul 18, 2024
Macular degeneration, X-linked atrophic1Nov 19, 2024
Malan overgrowth syndrome3Jul 18, 2024
Malignant hyperthermia, susceptibility to, 110Nov 19, 2024
Mandibular hypoplasia-deafness-progeroid syndrome1Dec 21, 2022
Mandibuloacral dysplasia with type A lipodystrophy1Nov 19, 2024
Mandibulofacial dysostosis-microcephaly syndrome10Nov 19, 2024
Maple syrup urine disease2Dec 21, 2022
Marden-Walker syndrome1Nov 19, 2024
Marfan syndrome52Nov 19, 2024
Marshall syndrome2Nov 19, 2024
Martsolf syndrome 12Dec 21, 2022
Mast syndrome1Jul 18, 2024
Maturity-onset diabetes of the young type 11Nov 19, 2024
Maturity-onset diabetes of the young type 25Nov 19, 2024
Maturity-onset diabetes of the young type 35Nov 19, 2024
Maturity-onset diabetes of the young type 91Jul 18, 2024
McCune-Albright syndrome2Nov 19, 2024
Meckel syndrome, type 62Nov 19, 2024
Meckel-Gruber syndrome1Dec 21, 2022
Medium-chain acyl-coenzyme A dehydrogenase deficiency6Nov 19, 2024
Meester-Loeys syndrome2Nov 19, 2024
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations5Nov 19, 2024
Megabladder, congenital1Nov 19, 2024
Megalencephalic leukoencephalopathy with subcortical cysts 12Jul 18, 2024
Megalencephaly-capillary malformation-polymicrogyria syndrome3Jul 18, 2024
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 11Dec 21, 2022
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 21Jul 18, 2024
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 33Jul 18, 2024
Megalocornea1Nov 1, 2016
Melnick-Fraser syndrome1Dec 21, 2022
Melnick-Needles syndrome1Nov 19, 2024
Menke-Hennekam syndrome 11Nov 19, 2024
Menke-Hennekam syndrome 22Jul 18, 2024
Menkes kinky-hair syndrome9Nov 19, 2024
Merosin deficient congenital muscular dystrophy1Nov 19, 2024
Metachromatic leukodystrophy5Jul 18, 2024
Metachromatic leukodystrophy, juvenile type1Dec 21, 2022
Metaphyseal chondrodysplasia, McKusick type4Jul 18, 2024
Metaphyseal chondrodysplasia, Schmid type3Jul 18, 2024
Methylmalonate semialdehyde dehydrogenase deficiency1Jul 18, 2024
Methylmalonic acidemia with homocystinuria, type cblX5Jul 18, 2024
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency1Nov 19, 2024
Methylmalonic aciduria, cblB type2Jul 18, 2024
Mevalonic aciduria4Nov 19, 2024
Microcephalic osteodysplastic primordial dwarfism type II1Dec 21, 2022
Microcephalic primordial dwarfism due to RTTN deficiency8Nov 19, 2024
Microcephalic primordial dwarfism due to ZNF335 deficiency5Jul 18, 2024
Microcephalic primordial dwarfism, Alazami type2Jul 18, 2024
Microcephaly 1, primary, autosomal recessive4Dec 21, 2022
Microcephaly 13, primary, autosomal recessive1Dec 21, 2022
Microcephaly 15, primary, autosomal recessive3Jul 18, 2024
Microcephaly 16, primary, autosomal recessive1Jul 18, 2024
Microcephaly 17, primary, autosomal recessive2Dec 21, 2022
Microcephaly 18, primary, autosomal dominant5Nov 19, 2024
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations7Jul 18, 2024
Microcephaly 20, primary, autosomal recessive4Jul 18, 2024
Microcephaly 26, primary, autosomal dominant1Jul 18, 2024
Microcephaly 5, primary, autosomal recessive16Nov 19, 2024
Microcephaly 8, primary, autosomal recessive1Dec 21, 2022
Microcephaly and chorioretinopathy 16Nov 19, 2024
Microcephaly and chorioretinopathy 31Jul 18, 2024
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability5Jul 18, 2024
Microcephaly, developmental delay, and brittle hair syndrome2Jul 18, 2024
Microcephaly, growth deficiency, seizures, and brain malformations1Dec 21, 2022
Microcephaly, growth restriction, and increased sister chromatid exchange 25Nov 19, 2024
Microcephaly, normal intelligence and immunodeficiency1Nov 19, 2024
Microcephaly, seizures, and developmental delay4Nov 19, 2024
Microcephaly, short stature, and impaired glucose metabolism 11Nov 19, 2024
Microcephaly, short stature, and limb abnormalities4Nov 19, 2024
Microcephaly-capillary malformation syndrome2Nov 19, 2024
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome4Jul 18, 2024
Microcephaly-thin corpus callosum-intellectual disability syndrome3Dec 21, 2022
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome14Nov 19, 2024
Microphthalmia with brain and digit anomalies1Jul 18, 2024
Microphthalmia, isolated, with coloboma 93Jul 18, 2024
Microphthalmia, syndromic 123Nov 19, 2024
Migraine, familial hemiplegic, 11Dec 21, 2022
Migraine, familial hemiplegic, 22Jul 18, 2024
Migraine, with or without aura, susceptibility to, 131Dec 21, 2022
Mirror movements 13Nov 19, 2024
Mitochondrial DNA deletion syndrome with progressive myopathy1Nov 19, 2024
Mitochondrial DNA depletion syndrome 14Jul 18, 2024
Mitochondrial DNA depletion syndrome 135Nov 19, 2024
Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)1Nov 19, 2024
Mitochondrial DNA depletion syndrome 20 (mngie type)1Jul 18, 2024
Mitochondrial DNA depletion syndrome 4b2Nov 19, 2024
Mitochondrial DNA depletion syndrome 8a1Nov 19, 2024
Mitochondrial DNA depletion syndrome 91Dec 21, 2022
Mitochondrial DNA depletion syndrome, myopathic form2Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 102Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 111Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 141Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 161Oct 1, 2019
Mitochondrial complex 1 deficiency, nuclear type 173Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 193Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 22Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 211Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 222Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 231Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 241Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 251Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 263Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 282Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 32Nov 19, 2024
Mitochondrial complex 1 deficiency, nuclear type 341Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 42Dec 21, 2022
Mitochondrial complex 1 deficiency, nuclear type 54Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 61Jul 18, 2024
Mitochondrial complex 1 deficiency, nuclear type 71Dec 21, 2022
Mitochondrial complex 2 deficiency, nuclear type 22Dec 21, 2022
Mitochondrial complex 2 deficiency, nuclear type 41Nov 19, 2024
Mitochondrial complex 4 deficiency, nuclear type 112Nov 19, 2024
Mitochondrial complex 4 deficiency, nuclear type 211Jul 18, 2024
Mitochondrial complex II deficiency, nuclear type 14Nov 19, 2024
Mitochondrial complex III deficiency nuclear type 13Jul 18, 2024
Mitochondrial complex IV deficiency, nuclear type 14Nov 19, 2024
Mitochondrial disease19Nov 19, 2024
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency1Jul 18, 2024
Mitochondrial myopathy-lactic acidosis-deafness syndrome3Dec 21, 2022
Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency11Nov 19, 2024
Monosomy 7 myelodysplasia and leukemia syndrome 23Nov 19, 2024
Mosaic variegated aneuploidy syndrome 12Dec 21, 2022
Mosaic variegated aneuploidy syndrome 32Dec 21, 2022
Mowat-Wilson syndrome5Nov 19, 2024
Moyamoya disease 23Nov 19, 2024
Mucopolysaccharidosis type 11Dec 21, 2022
Mucopolysaccharidosis type 62Jul 18, 2024
Mucopolysaccharidosis type 72Dec 21, 2022
Mucopolysaccharidosis, MPS-II3Jul 18, 2024
Mucopolysaccharidosis, MPS-III-A4Jul 18, 2024
Mucopolysaccharidosis, MPS-III-B1Nov 19, 2024
Mucopolysaccharidosis, MPS-III-C2Jul 18, 2024
Mucopolysaccharidosis, MPS-III-D1Nov 19, 2024
Mucopolysaccharidosis, MPS-IV-A2Jul 18, 2024
Muenke syndrome2Nov 19, 2024
Mullegama-Klein-Martinez syndrome3Nov 19, 2024
Multiple acyl-CoA dehydrogenase deficiency7Nov 19, 2024
Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type1Jul 18, 2024
Multiple congenital anomalies-hypotonia-seizures syndrome 14Nov 19, 2024
Multiple congenital anomalies-hypotonia-seizures syndrome 23Jul 18, 2024
Multiple congenital anomalies-hypotonia-seizures syndrome 31Jul 18, 2024
Multiple congenital anomalies-neurodevelopmental syndrome, X-linked1Jul 18, 2024
Multiple congenital anomalies/dysmorphic syndrome1Jul 18, 2024
Multiple endocrine neoplasia type 2A1Dec 21, 2022
Multiple endocrine neoplasia, type 12Jul 18, 2024
Multiple endocrine neoplasia, type 21Nov 19, 2024
Multiple gastrointestinal atresias1Nov 1, 2016
Multiple mitochondrial dysfunctions syndrome 21Oct 1, 2019
Multiple mitochondrial dysfunctions syndrome 31Dec 21, 2022
Multiple mitochondrial dysfunctions syndrome 63Dec 21, 2022
Multiple self-healing squamous epithelioma1Dec 21, 2022
Multiple synostoses syndrome 31Dec 21, 2022
Multisystemic smooth muscle dysfunction syndrome2Jul 18, 2024
Muscular dystrophy1Nov 19, 2024
Muscular dystrophy, limb-girdle, autosomal dominant 42Nov 19, 2024
Muscular dystrophy, limb-girdle, autosomal recessive 233Jul 18, 2024
Muscular dystrophy-dystroglycanopathy1Jul 18, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 42Jul 18, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 72Nov 19, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A16Nov 19, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A141Nov 19, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A52Jul 18, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A91Jul 18, 2024
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 101Dec 21, 2022
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 111Dec 21, 2022
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 121Dec 21, 2022
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B141Jul 18, 2024
Myasthenic syndrome, congenital, 24, presynaptic1Dec 21, 2022
Myasthenic syndrome, congenital, 25, presynaptic1Dec 21, 2022
Myhre syndrome3Nov 19, 2024
Myoclonic dystonia 112Nov 19, 2024
Myoclonic-astatic epilepsy3Dec 21, 2022
Myoclonic-atonic epilepsy4Nov 19, 2024
Myofibrillar myopathy 111Nov 19, 2024
Myofibrillar myopathy 31Nov 19, 2024
Myofibrillar myopathy 41Dec 21, 2022
Myofibrillar myopathy 51Dec 21, 2022
Myopathy caused by variation in FKTN2Dec 21, 2022
Myopathy caused by variation in POMGNT12Dec 21, 2022
Myopathy caused by variation in POMT11Dec 21, 2022
Myopathy, centronuclear, 51Dec 21, 2022
Myopathy, distal, 51Nov 19, 2024
Myopathy, distal, with rimmed vacuoles1Nov 19, 2024
Myopathy, myofibrillar, 9, with early respiratory failure1Nov 19, 2024
Myopathy, proximal, and ophthalmoplegia5Nov 19, 2024
Myopia, high, with cataract and vitreoretinal degeneration1Nov 19, 2024
NAD(P)HX dehydratase deficiency4Nov 19, 2024
Naegeli-Franceschetti-Jadassohn syndrome1Nov 19, 2024
Nail-patella syndrome3Nov 19, 2024
Namaqualand hip dysplasia1Jul 18, 2024
Nance-Horan syndrome1Dec 21, 2022
Nemaline myopathy 101Dec 21, 2022
Nemaline myopathy 212Nov 19, 2024
Nemaline myopathy 61Jul 18, 2024
Nemaline myopathy 84Nov 19, 2024
Neonatal intrahepatic cholestasis due to citrin deficiency2Dec 21, 2022
Neonatal pseudo-hydrocephalic progeroid syndrome1Nov 19, 2024
Neonatal severe primary hyperparathyroidism2Nov 19, 2024
Neonatal-onset encephalopathy with rigidity and seizures4Nov 19, 2024
Neonatal/infantile epilepsy syndrome1Nov 19, 2024
Nephrogenic syndrome of inappropriate antidiuresis1Dec 21, 2022
Nephrolithiasis susceptibility caused by SLC26A11Nov 19, 2024
Nephronophthisis 13Jul 18, 2024
Nephronophthisis 181Nov 19, 2024
Nephronophthisis 201Dec 21, 2022
Nephronophthisis 35Nov 19, 2024
Nephronophthisis 42Dec 21, 2022
Nephropathic cystinosis1Apr 4, 2023
Nephrotic syndrome6Nov 19, 2024
Nephrotic syndrome 142Jul 18, 2024
Nephrotic syndrome 151Dec 21, 2022
Nephrotic syndrome, IIa 262Nov 19, 2024
Nephrotic syndrome, type 111Nov 19, 2024
Nephrotic syndrome, type 26Jul 18, 2024
Nephrotic syndrome, type 201Nov 19, 2024
Nephrotic syndrome, type 33Jul 18, 2024
Nephrotic syndrome, type 42Nov 19, 2024
Netherton syndrome4Jul 18, 2024
Neu-Laxova syndrome 22Dec 21, 2022
Neurodegeneration with brain iron accumulation 2B2Jul 18, 2024
Neurodegeneration with brain iron accumulation 43Nov 19, 2024
Neurodegeneration with brain iron accumulation 54Nov 19, 2024
Neurodegeneration with brain iron accumulation 62Jul 18, 2024
Neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities2Jul 18, 2024
Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia2Oct 1, 2019
Neurodegeneration, infantile-onset, biotin-responsive2Dec 21, 2022
Neurodevelopmental disorder156Nov 19, 2024
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity3Jul 18, 2024
Neurodevelopmental disorder with absent language and variable seizures2Nov 19, 2024
Neurodevelopmental disorder with alopecia and brain abnormalities1Jul 18, 2024
Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter3Jul 18, 2024
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia1Jul 18, 2024
Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies2Nov 19, 2024
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies7Nov 19, 2024
Neurodevelopmental disorder with central and peripheral motor dysfunction1Dec 21, 2022
Neurodevelopmental disorder with central hypotonia and dysmorphic facies2Nov 19, 2024
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction1Nov 19, 2024
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures3Dec 21, 2022
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities7Nov 19, 2024
Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects1Nov 19, 2024
Neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities1Nov 19, 2024
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies10Nov 19, 2024
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies4Jul 18, 2024
Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum3Nov 19, 2024
Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia1Dec 21, 2022
Neurodevelopmental disorder with epilepsy and brain atrophy2Nov 19, 2024
Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy1Dec 21, 2022
Neurodevelopmental disorder with eye movement abnormalities and ataxia1Jul 18, 2024
Neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked1Nov 19, 2024
Neurodevelopmental disorder with hearing loss and spasticity1Jul 18, 2024
Neurodevelopmental disorder with hypotonia and brain abnormalities1Nov 19, 2024
Neurodevelopmental disorder with hypotonia and dysmorphic facies1Dec 21, 2022
Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities1Dec 21, 2022
Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language1Nov 19, 2024
Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures2Nov 19, 2024
Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities1Oct 1, 2019
Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities1Nov 19, 2024
Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures3Nov 19, 2024
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness4Jul 18, 2024
Neurodevelopmental disorder with hypotonia, seizures, and absent language10Nov 19, 2024
Neurodevelopmental disorder with impaired language and ataxia and with or without seizures1Nov 19, 2024
Neurodevelopmental disorder with impaired speech and hyperkinetic movements4Nov 19, 2024
Neurodevelopmental disorder with infantile epileptic spasms1Dec 21, 2022
Neurodevelopmental disorder with involuntary movements1Dec 21, 2022
Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures2Nov 19, 2024
Neurodevelopmental disorder with language delay and variable cognitive abnormalities1Nov 19, 2024
Neurodevelopmental disorder with language impairment and behavioral abnormalities2Nov 19, 2024
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies3Dec 21, 2022
Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy1Dec 21, 2022
Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies1Nov 19, 2024
Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities3Nov 19, 2024
Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy1Nov 19, 2024
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities1Nov 19, 2024
Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures3Nov 19, 2024
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart12Jul 18, 2024
Neurodevelopmental disorder with or without autism or seizures4Nov 19, 2024
Neurodevelopmental disorder with or without early-onset generalized epilepsy11Nov 19, 2024
Neurodevelopmental disorder with or without variable brain abnormalities; NEDBA3Dec 21, 2022
Neurodevelopmental disorder with poor language and loss of hand skills1Jul 18, 2024
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies1Dec 21, 2022
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities2Jul 18, 2024
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures7Nov 19, 2024
Neurodevelopmental disorder with seizures and brain atrophy1Dec 21, 2022
Neurodevelopmental disorder with seizures and speech and walking impairment2Nov 19, 2024
Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities2Jul 18, 2024
Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities1Jul 18, 2024
Neurodevelopmental disorder with severe motor impairment and absent language3Nov 19, 2024
Neurodevelopmental disorder with speech delay and variable ocular anomalies1Jul 18, 2024
Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies1Dec 21, 2022
Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures1Dec 21, 2022
Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus2Dec 21, 2022
Neurofibromatosis, type 127Nov 19, 2024
Neurofibromatosis, type 22Jul 18, 2024
Neurofibromatosis-Noonan syndrome2Jun 18, 2024
Neurohypophyseal diabetes insipidus1Jul 18, 2024
Neuromuscular disease and ocular or auditory anomalies with or without seizures1Dec 21, 2022
Neuronal ceroid lipofuscinosis 13Jul 18, 2024
Neuronal ceroid lipofuscinosis 101Jul 18, 2024
Neuronal ceroid lipofuscinosis 24Nov 19, 2024
Neuronal ceroid lipofuscinosis 32Jul 18, 2024
Neuronal ceroid lipofuscinosis 74Jul 18, 2024
Neuronopathy, distal hereditary motor, autosomal dominant 101Nov 19, 2024
Neuronopathy, distal hereditary motor, autosomal recessive 51Nov 19, 2024
Neuronopathy, distal hereditary motor, autosomal recessive 71Jul 18, 2024
Neuronopathy, distal hereditary motor, autosomal recessive 82Jul 18, 2024
Neuronopathy, distal hereditary motor, type 2B1Nov 19, 2024
Neuronopathy, distal hereditary motor, type 5C1Nov 19, 2024
Neuroocular syndrome 12Jul 18, 2024
Neurooculocardiogenitourinary syndrome1Dec 21, 2022
Neuropathy, congenital hypomyelinating, 32Nov 19, 2024
Neuropathy, hereditary motor and sensory, type 6A2Nov 19, 2024
Neuropathy, hereditary sensory and autonomic, type 1A1Jul 18, 2024
Neuropathy, hereditary sensory and autonomic, type 1C1Jul 18, 2024
Neuropathy, hereditary sensory and autonomic, type 2A1Nov 19, 2024
Neuropathy, hereditary sensory, type 1F1Jul 18, 2024
Neuropathy, hereditary sensory, type 2C2Nov 19, 2024
Neutral lipid storage myopathy3Jul 18, 2024
Neutropenia, severe congenital, 1, autosomal dominant2Nov 19, 2024
Neutropenia, severe congenital, 2, autosomal dominant1Jul 18, 2024
Neutropenia, severe congenital, 8, autosomal dominant1Nov 19, 2024
Nicolaides-Baraitser syndrome11Nov 19, 2024
Niemann-Pick disease, type A1Jul 18, 2024
Niemann-Pick disease, type C115Nov 19, 2024
Nizon-Isidor syndrome1Dec 21, 2022
Non-immune hydrops fetalis1Nov 19, 2024
Non-ketotic hyperglycinemia1Dec 21, 2022
Non-syndromic X-linked intellectual disability2Nov 19, 2024
Non-syndromic renal or urinary tract malformation1Aug 3, 2022
Nonsyndromic genetic hearing loss5Nov 19, 2024
Noonan syndrome1Dec 21, 2022
Noonan syndrome 134Nov 19, 2024
Noonan syndrome 108Nov 19, 2024
Noonan syndrome 111Jul 18, 2024
Noonan syndrome 122Jul 18, 2024
Noonan syndrome 131Nov 19, 2024
Noonan syndrome 27Nov 19, 2024
Noonan syndrome 33Nov 19, 2024
Noonan syndrome 411Nov 19, 2024
Noonan syndrome 510Nov 19, 2024
Noonan syndrome 63Nov 19, 2024
Noonan syndrome 71Jul 18, 2024
Noonan syndrome 88Jul 18, 2024
Noonan syndrome 94Jul 18, 2024
Noonan syndrome-like disorder with loose anagen hair 12Jul 18, 2024
Noonan syndrome-like disorder with loose anagen hair 22Jul 18, 2024
Norman-Roberts syndrome1Nov 19, 2024
Normophosphatemic familial tumoral calcinosis1Nov 19, 2024
Nystagmus 1, congenital, X-linked3Nov 19, 2024
O'Donnell-Luria-Rodan syndrome6Nov 19, 2024
Obesity due to SIM1 deficiency1Jul 18, 2024
Obesity due to melanocortin 4 receptor deficiency1Nov 19, 2024
Obesity due to prohormone convertase I deficiency1Nov 19, 2024
Obesity, hyperphagia, and developmental delay1Nov 19, 2024
Occult macular dystrophy1Nov 19, 2024
Ocular albinism, type I1Nov 19, 2024
Oculocerebrofacial syndrome, Kaufman type2Dec 21, 2022
Oculocutaneous albinism3Nov 19, 2024
Oculocutaneous albinism type 1B3Nov 19, 2024
Oculocutaneous albinism type 44Nov 19, 2024
Oculodentodigital dysplasia1Nov 19, 2024
Oculofaciocardiodental syndrome3Jul 18, 2024
Oculogastrointestinal-neurodevelopmental syndrome1Nov 19, 2024
Oculomotor apraxia - Cogan type1Nov 19, 2024
Ogden syndrome2Nov 19, 2024
Oguchi disease-11Jul 18, 2024
Okur-Chung neurodevelopmental syndrome3Nov 19, 2024
Optic atrophy1Nov 19, 2024
Optic atrophy 121Nov 19, 2024
Optic atrophy 31Nov 19, 2024
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy8Nov 19, 2024
Ornithine aminotransferase deficiency2Jul 18, 2024
Ornithine carbamoyltransferase deficiency6Nov 19, 2024
Orofacial cleft 111Dec 21, 2022
Orofaciodigital syndrome 171Jul 18, 2024
Orofaciodigital syndrome I4Nov 19, 2024
Orofaciodigital syndrome type 142Dec 21, 2022
Orofaciodigital syndrome type 63Jul 18, 2024
Osteodysplastic primordial dwarfism, type 11Dec 21, 2022
Osteogenesis imperfecta2Nov 19, 2024
Osteogenesis imperfecta type 111Dec 21, 2022
Osteogenesis imperfecta type 51Jul 18, 2024
Osteogenesis imperfecta type 72Dec 21, 2022
Osteogenesis imperfecta type 82Dec 21, 2022
Osteogenesis imperfecta type I17Jul 18, 2024
Osteogenesis imperfecta type III1Dec 21, 2022
Osteogenesis imperfecta with normal sclerae, dominant form5Nov 19, 2024
Osteogenesis imperfecta, perinatal lethal8Nov 19, 2024
Osteopathia striata with cranial sclerosis1Nov 19, 2024
Osteoporosis2Nov 19, 2024
Osteoporosis with pseudoglioma2Nov 19, 2024
Osteoporosis, childhood- or juvenile-onset, with developmental delay1Nov 19, 2024
Oto-palato-digital syndrome, type I1Nov 19, 2024
Otofaciocervical syndrome 23Nov 19, 2024
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes1Jul 18, 2024
PERCHING syndrome2Nov 19, 2024
PHGDH deficiency1Jul 18, 2024
PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome8Nov 19, 2024
PIGG-related neurodevelopmental disorder1Oct 1, 2019
PIK3CA related overgrowth syndrome1Dec 21, 2022
PLA2G6-associated neurodegeneration1Nov 19, 2024
PMM2-congenital disorder of glycosylation11Nov 19, 2024
PRRT2-associated paroxysmal movement disorder2Nov 19, 2024
PTEN hamartoma tumor syndrome13Nov 19, 2024
PTPN23-related neurodevelopmental disorder1Oct 1, 2019
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome5Nov 19, 2024
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation5Jul 18, 2024
Pachyonychia congenita 31Nov 19, 2024
Paget disease of bone 61Jul 18, 2024
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome9Nov 19, 2024
Palmoplantar keratoderma, nonepidermolytic, focal 11Jul 18, 2024
Palmoplantar keratoderma, punctate type 1A2Jul 18, 2024
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome1Dec 21, 2022
Paragangliomas 53Nov 19, 2024
Parenti-mignot neurodevelopmental syndrome4Nov 19, 2024
Paroxysmal extreme pain disorder1Nov 19, 2024
Paroxysmal nonkinesigenic dyskinesia 11Dec 21, 2022
Partial androgen insensitivity syndrome3Nov 19, 2024
Patent ductus arteriosus 31Nov 19, 2024
Patterned macular dystrophy 11Nov 19, 2024
Pearson syndrome2Jun 12, 2019
Pelger-Huët anomaly1Nov 1, 2016
Pelizaeus-Merzbacher disease2Nov 19, 2024
Pendred syndrome9Nov 19, 2024
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development2Dec 21, 2022
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome1Jul 18, 2024
Periventricular heterotopia with microcephaly, autosomal recessive3Jul 18, 2024
Periventricular nodular heterotopia1Nov 19, 2024
Periventricular nodular heterotopia 81Jul 18, 2024
Periventricular nodular heterotopia 93Jul 18, 2024
Perlman syndrome2Dec 21, 2022
Peroxisome biogenesis disorder2Dec 21, 2022
Peroxisome biogenesis disorder 14B1Dec 21, 2022
Peroxisome biogenesis disorder 1A (Zellweger)2Jul 18, 2024
Peroxisome biogenesis disorder 2B1Jul 18, 2024
Peroxisome biogenesis disorder 4A (Zellweger)4Nov 19, 2024
Peroxisome biogenesis disorder 4B3Nov 19, 2024
Peroxisome biogenesis disorder 6B1Dec 21, 2022
Peroxisome biogenesis disorder due to PEX1 defect5Nov 19, 2024
Peroxisome biogenesis disorder due to PEX16 defect1Dec 21, 2022
Perrault syndrome 11Dec 21, 2022
Perrault syndrome 21Nov 19, 2024
Perrault syndrome 41Jul 18, 2024
Perrault syndrome 51Nov 19, 2024
Perry syndrome1Nov 19, 2024
Persistent Mullerian duct syndrome2Nov 19, 2024
Pfeiffer syndrome1Nov 19, 2024
Phelan-McDermid syndrome2Nov 19, 2024
Phenylketonuria19Nov 19, 2024
Pierson syndrome1Jul 18, 2024
Pigmentary retinal dystrophy1Dec 21, 2022
Pilarowski-Bjornsson syndrome6Nov 19, 2024
Pili torti-deafness syndrome1Nov 19, 2024
Pitt-Hopkins syndrome13Nov 19, 2024
Pitt-Hopkins-like syndrome1Dec 21, 2022
Platelet-type bleeding disorder 153Nov 19, 2024
Platelet-type bleeding disorder 171Nov 19, 2024
Poikiloderma with neutropenia1Dec 21, 2022
Poirier-Bienvenu neurodevelopmental syndrome5Nov 19, 2024
Polycystic kidney disease 248Nov 19, 2024
Polycystic kidney disease 3 with or without polycystic liver disease8Nov 19, 2024
Polycystic kidney disease 464Nov 19, 2024
Polycystic kidney disease 52Jul 18, 2024
Polycystic kidney disease 6 with or without polycystic liver disease3Nov 19, 2024
Polycystic kidney disease, adult type262Nov 19, 2024
Polycystic liver disease 13Nov 19, 2024
Polycystic liver disease 27Nov 19, 2024
Polycystic liver disease 3 with or without kidney cysts1Nov 19, 2024
Polydactyly, postaxial, type A11Jul 18, 2024
Polydactyly, postaxial, type a73Nov 19, 2024
Polyendocrine-polyneuropathy syndrome1Nov 19, 2024
Polyglandular autoimmune syndrome, type 12Nov 19, 2024
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis4Jul 18, 2024
Polysyndactyly 41Jul 18, 2024
Pontocerebellar hypoplasia type 1B3Jul 18, 2024
Pontocerebellar hypoplasia type 2A1Jul 18, 2024
Pontocerebellar hypoplasia type 31Jul 18, 2024
Pontocerebellar hypoplasia type 66Nov 19, 2024
Pontocerebellar hypoplasia type 72Jul 18, 2024
Pontocerebellar hypoplasia type 81Nov 19, 2024
Pontocerebellar hypoplasia type 92Aug 30, 2020
Pontocerebellar hypoplasia, type 161Nov 19, 2024
Pontocerebellar hypoplasia, type 1D1Jul 18, 2024
Porencephaly 28Nov 19, 2024
Porokeratosis 7, multiple types1Nov 19, 2024
Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome1Dec 21, 2022
Posterior column ataxia-retinitis pigmentosa syndrome2Nov 19, 2024
Potassium-aggravated myotonia1Nov 19, 2024
Precocious puberty, central, 21Nov 19, 2024
Predisposition to invasive fungal disease due to CARD9 deficiency1Aug 3, 2022
Premature ovarian failure 141Dec 21, 2022
Premature ovarian failure 51Nov 19, 2024
Premature ovarian insufficiency2Sep 16, 2020
Prieto syndrome1Nov 19, 2024
Primary ciliary dyskinesia 111Dec 21, 2022
Primary ciliary dyskinesia 142Dec 21, 2022
Primary ciliary dyskinesia 152Nov 19, 2024
Primary ciliary dyskinesia 221Dec 21, 2022
Primary ciliary dyskinesia 231Nov 19, 2024
Primary ciliary dyskinesia 252Nov 19, 2024
Primary ciliary dyskinesia 262Nov 19, 2024
Primary ciliary dyskinesia 271Dec 21, 2022
Primary ciliary dyskinesia 35Jul 18, 2024
Primary ciliary dyskinesia 341Nov 19, 2024
Primary ciliary dyskinesia 51Nov 19, 2024
Primary ciliary dyskinesia 78Jul 18, 2024
Primary coenzyme Q10 deficiency 82Nov 19, 2024
Primary dilated cardiomyopathy22Nov 19, 2024
Primary hyperoxaluria type 33Nov 19, 2024
Primary hyperoxaluria, type I7Nov 19, 2024
Primary hyperoxaluria, type II4Nov 19, 2024
Primary hypomagnesemia1Aug 30, 2020
Primrose syndrome4Nov 19, 2024
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 12Nov 19, 2024
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 33Nov 19, 2024
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 41Nov 19, 2024
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 53Nov 19, 2024
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 11Nov 19, 2024
Progressive familial heart block type IB1Nov 19, 2024
Progressive familial intrahepatic cholestasis type 21Dec 21, 2022
Progressive familial intrahepatic cholestasis type 36Nov 19, 2024
Progressive myoclonic epilepsy type 32Jul 18, 2024
Progressive osseous heteroplasia1Nov 19, 2024
Progressive pseudorheumatoid dysplasia2Jul 18, 2024
Progressive sclerosing poliodystrophy6Nov 19, 2024
Progressive supranuclear palsy-parkinsonism syndrome2Nov 19, 2024
Propionic acidemia3Nov 19, 2024
Proteinuria, chronic benign6Nov 19, 2024
Protoporphyria, erythropoietic, 14Nov 19, 2024
Proximal myopathy with extrapyramidal signs1Jul 18, 2024
Pseudohypoaldosteronism type 2E1Jul 18, 2024
Pseudohypoaldosteronism, type IB1, autosomal recessive1Jul 18, 2024
Pseudohypoparathyroidism type I A6Nov 19, 2024
Psoriasis 21Dec 21, 2022
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome1Nov 19, 2024
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 11Nov 19, 2024
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 33Nov 19, 2024
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 43Nov 19, 2024
Pulmonary hypertension, primary, 14Jul 18, 2024
Purine-nucleoside phosphorylase deficiency1Jul 18, 2024
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome1Dec 21, 2022
Pyridoxal phosphate-responsive seizures3Nov 19, 2024
Pyridoxine-dependent epilepsy5Nov 19, 2024
Pyruvate dehydrogenase E1-alpha deficiency11Nov 19, 2024
Pyruvate dehydrogenase E2 deficiency1Nov 19, 2024
Pyruvate dehydrogenase E3 deficiency1Dec 21, 2022
Pyruvate kinase deficiency of red cells3Nov 19, 2024
Qualitative or quantitative defects of perlecan1Jul 18, 2024
RAB23-related Carpenter syndrome1Jul 18, 2024
RFT1-congenital disorder of glycosylation2Jul 18, 2024
RNU4ATAC spectrum disorder1Nov 19, 2024
RYR1-related myopathy25Nov 19, 2024
Radial aplasia-thrombocytopenia syndrome1Jul 18, 2024
Radio-Tartaglia syndrome5Jul 18, 2024
Radioulnar synostosis with amegakaryocytic thrombocytopenia 23Jul 18, 2024
Rafiq syndrome2Jul 18, 2024
Rahman syndrome1Nov 19, 2024
Rapp-Hodgkin syndrome1Nov 19, 2024
Rauch-Steindl syndrome5Nov 19, 2024
Recessive dystrophic epidermolysis bullosa13Nov 19, 2024
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome4Jul 18, 2024
Renal carnitine transport defect2Jul 18, 2024
Renal coloboma syndrome1Jul 18, 2024
Renal cyst15Nov 19, 2024
Renal cysts and diabetes syndrome20Nov 19, 2024
Renal hypodysplasia/aplasia 32Nov 19, 2024
Renal hypomagnesemia 5 with ocular involvement1Jul 18, 2024
Renal tubular acidosis with progressive nerve deafness3Jul 18, 2024
Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss1Nov 19, 2024
Renal tubular acidosis, distal, 4, with hemolytic anemia1Nov 19, 2024
Renpenning syndrome1Nov 19, 2024
Restrictive dermopathy 12Jul 18, 2024
Reticular dysgenesis1Jul 18, 2024
Retinal dystrophy with or without macular staphyloma2Nov 19, 2024
Retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome1Jul 18, 2024
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations1Nov 19, 2024
Retinitis pigmentosa1Nov 19, 2024
Retinitis pigmentosa 11Nov 19, 2024
Retinitis pigmentosa 101Dec 21, 2022
Retinitis pigmentosa 114Nov 19, 2024
Retinitis pigmentosa 124Nov 19, 2024
Retinitis pigmentosa 131Dec 21, 2022
Retinitis pigmentosa 21Nov 19, 2024
Retinitis pigmentosa 254Jul 18, 2024
Retinitis pigmentosa 262Dec 21, 2022
Retinitis pigmentosa 32Nov 19, 2024
Retinitis pigmentosa 301Dec 21, 2022
Retinitis pigmentosa 311Dec 21, 2022
Retinitis pigmentosa 333Nov 19, 2024
Retinitis pigmentosa 372Nov 19, 2024
Retinitis pigmentosa 394Jul 18, 2024
Retinitis pigmentosa 44Nov 19, 2024
Retinitis pigmentosa 433Jul 18, 2024
Retinitis pigmentosa 561Nov 19, 2024
Retinitis pigmentosa 591Nov 19, 2024
Retinitis pigmentosa 702Dec 21, 2022
Retinitis pigmentosa 711Dec 21, 2022
Retinitis pigmentosa 781Dec 21, 2022
Retinitis pigmentosa 882Nov 19, 2024
Retinoblastoma2Nov 19, 2024
Rett syndrome20Nov 19, 2024
Rett syndrome, congenital variant5Jul 18, 2024
Rhabdoid tumor predisposition syndrome 21Nov 19, 2024
Rhizomelic chondrodysplasia punctata type 12Nov 19, 2024
Rienhoff syndrome1Jul 18, 2024
Right atrial isomerism1Nov 19, 2024
Ritscher-Schinzel syndrome 11Nov 19, 2024
Ritscher-Schinzel syndrome 24Nov 19, 2024
Roifman syndrome4Jul 18, 2024
Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked1Jul 18, 2024
Rothmund-Thomson syndrome type 24Dec 21, 2022
Rubinstein-Taybi syndrome due to CREBBP mutations20Nov 19, 2024
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency9Nov 19, 2024
SATB2 associated disorder3Jul 18, 2024
SCN4A-related myopathy, autosomal recessive5Nov 19, 2024
SIN3A-related intellectual disability syndrome3Jul 18, 2024
SIN3A-related intellectual disability syndrome due to a point mutation3Nov 19, 2024
SLC35A2-congenital disorder of glycosylation1Dec 21, 2022
SLC39A8-CDG1Dec 21, 2022
SRD5A3-congenital disorder of glycosylation2Nov 19, 2024
SSR4-congenital disorder of glycosylation2Nov 19, 2024
STING-associated vasculopathy with onset in infancy2Nov 19, 2024
STT3A-congenital disorder of glycosylation1Nov 19, 2024
Saethre-Chotzen syndrome2Nov 19, 2024
Saldino-Mainzer syndrome2Nov 19, 2024
Sandestig-stefanova syndrome2Jul 18, 2024
Sandhoff disease2Nov 19, 2024
Scalp-ear-nipple syndrome1Jul 18, 2024
Schaaf-Yang syndrome8Nov 19, 2024
Schimke immuno-osseous dysplasia2Dec 21, 2022
Schinzel-Giedion syndrome6Nov 19, 2024
Schnyder crystalline corneal dystrophy1Nov 19, 2024
Schuurs-Hoeijmakers syndrome2Nov 19, 2024
Schwannomatosis 24Nov 19, 2024
Schwartz-Jampel syndrome type 13Nov 19, 2024
Seckel syndrome 21Jul 18, 2024
Seizures, benign familial infantile, 22Jul 18, 2024
Seizures, benign familial neonatal, 15Nov 19, 2024
Seizures, benign familial neonatal, 21Nov 19, 2024
Seizures, early-onset, with neurodegeneration and brain calcifications1Jul 18, 2024
Self-limited familial infantile epilepsy1Nov 19, 2024
Sengers syndrome2Dec 21, 2022
Senior-Loken syndrome 41Nov 19, 2024
Septo-optic dysplasia sequence1Nov 8, 2022
Severe X-linked myotubular myopathy6Nov 19, 2024
Severe combined immunodeficiency due to DNA-PKcs deficiency1Dec 21, 2022
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency1Jul 18, 2024
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive1Nov 19, 2024
Severe dermatitis-multiple allergies-metabolic wasting syndrome1Nov 19, 2024
Severe early-childhood-onset retinal dystrophy25Nov 19, 2024
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome4Jul 18, 2024
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome2Dec 21, 2022
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome3Nov 19, 2024
Severe intellectual disability-progressive spastic diplegia syndrome13Jul 18, 2024
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome1Jul 18, 2024
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome2Jul 18, 2024
Severe myoclonic epilepsy in infancy9Nov 19, 2024
Severe neonatal-onset encephalopathy with microcephaly1Jul 18, 2024
Shashi-Pena syndrome4Nov 19, 2024
Short QT syndrome 71Jul 18, 2024
Short stature with nonspecific skeletal abnormalities1Nov 19, 2024
Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 12Jul 18, 2024
Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay3Nov 19, 2024
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome1Jul 18, 2024
Short stature-brachydactyly-obesity-global developmental delay syndrome2Jul 18, 2024
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome1Dec 21, 2022
Short stature-optic atrophy-Pelger-HuC+t anomaly syndrome2Nov 19, 2024
Short-rib thoracic dysplasia 10 with or without polydactyly3Dec 21, 2022
Short-rib thoracic dysplasia 15 with polydactyly2Dec 21, 2022
Short-rib thoracic dysplasia 21 without polydactyly1Nov 19, 2024
Short-rib thoracic dysplasia 7 with or without polydactyly2Dec 21, 2022
Shprintzen-Goldberg syndrome3Jul 18, 2024
Shukla-Vernon syndrome6Nov 19, 2024
Shwachman-Diamond syndrome 14Nov 19, 2024
Shwachman-Diamond syndrome 21Jul 18, 2024
Sialic acid storage disease, severe infantile type2Nov 19, 2024
Sialidosis type 22Dec 21, 2022
Sick sinus syndrome 12Nov 19, 2024
Sick sinus syndrome 2, autosomal dominant3Nov 19, 2024
Sifrim-Hitz-Weiss syndrome16Nov 19, 2024
Silver-Russell syndrome 32Nov 19, 2024
Simpson-Golabi-Behmel syndrome type 12Nov 19, 2024
Sinoatrial node dysfunction and deafness2Nov 19, 2024
Sitosterolemia 11Jul 18, 2024
Sitosterolemia 21Jul 18, 2024
Situs inversus1Dec 21, 2022
Sjögren-Larsson syndrome1Nov 19, 2024
Skeletal dysplasia, mild, with joint laxity and advanced bone age1Dec 21, 2022
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome1Dec 21, 2022
Skraban-Deardorff syndrome2Jul 18, 2024
Smith-Lemli-Opitz syndrome11Nov 19, 2024
Smith-Magenis syndrome3Jul 18, 2024
Snijders Blok-Campeau syndrome14Nov 19, 2024
Sotos syndrome22Nov 19, 2024
Southeast Asian ovalocytosis1Nov 19, 2024
Spastic ataxia 23Jul 18, 2024
Spastic ataxia 31Jul 18, 2024
Spastic ataxia 42Dec 21, 2022
Spastic ataxia 51Nov 19, 2024
Spastic paraplegia 52, autosomal recessive1Jul 18, 2024
Spastic paraplegia 79A, autosomal dominant, with ataxia1Nov 19, 2024
Spastic paraplegia, intellectual disability, nystagmus, and obesity6Nov 19, 2024
Spasticity-ataxia-gait anomalies syndrome1Dec 21, 2022
Spinal muscular atrophy6Nov 19, 2024
Spinal muscular atrophy with congenital bone fractures 22Nov 19, 2024
Spinocerebellar ataxia 27A1Jul 18, 2024
Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits5Nov 19, 2024
Spinocerebellar ataxia 451Nov 19, 2024
Spinocerebellar ataxia 472Nov 19, 2024
Spinocerebellar ataxia 482Nov 19, 2024
Spinocerebellar ataxia type 131Jul 18, 2024
Spinocerebellar ataxia type 141Jul 18, 2024
Spinocerebellar ataxia type 15/163Nov 19, 2024
Spinocerebellar ataxia type 19/223Jul 18, 2024
Spinocerebellar ataxia type 211Dec 21, 2022
Spinocerebellar ataxia type 231Dec 21, 2022
Spinocerebellar ataxia type 251Nov 19, 2024
Spinocerebellar ataxia type 262Jul 18, 2024
Spinocerebellar ataxia type 281Nov 19, 2024
Spinocerebellar ataxia type 297Nov 19, 2024
Spinocerebellar ataxia type 341Nov 19, 2024
Spinocerebellar ataxia type 381Dec 21, 2022
Spinocerebellar ataxia type 422Jul 18, 2024
Spinocerebellar ataxia type 52Nov 19, 2024
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 22Nov 19, 2024
Split hand-foot malformation 61Nov 19, 2024
Sponastrime dysplasia2Dec 21, 2022
Spondylocarpotarsal synostosis syndrome2Nov 19, 2024
Spondylocostal dysostosis 3, autosomal recessive1Nov 19, 2024
Spondyloepimetaphyseal dysplasia with multiple dislocations2Dec 21, 2022
Spondyloepimetaphyseal dysplasia, Bieganski type1Dec 21, 2022
Spondyloepiphyseal dysplasia congenita1Jul 18, 2024
Spondyloepiphyseal dysplasia with congenital joint dislocations1Jul 18, 2024
Spondylometaphyseal dysplasia - Sutcliffe type2Nov 19, 2024
Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome1Dec 21, 2022
Spongy degeneration of central nervous system2Nov 19, 2024
Squalene synthase deficiency1Dec 21, 2022
Stankiewicz-Isidor syndrome1Nov 19, 2024
Stargardt disease7Nov 19, 2024
Steatocystoma multiplex1Dec 21, 2022
Steel syndrome1Dec 21, 2022
Stickler syndrome1Nov 19, 2024
Stickler syndrome type 112Jul 18, 2024
Stickler syndrome type 28Nov 19, 2024
Stickler syndrome, type 43Nov 19, 2024
Stickler syndrome, type 53Nov 19, 2024
Stickler syndrome, type I, nonsyndromic ocular2Dec 21, 2022
Striatonigral degeneration, childhood-onset1Dec 21, 2022
Structural heart defects and renal anomalies syndrome1Dec 21, 2022
Subcortical band heterotopia1Nov 19, 2024
Succinate-semialdehyde dehydrogenase deficiency2Jul 18, 2024
Sucrase-isomaltase deficiency2Nov 19, 2024
Sudden cardiac failure, infantile6Jul 18, 2024
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A3Nov 19, 2024
Supravalvar aortic stenosis3Nov 19, 2024
Surfactant metabolism dysfunction, pulmonary, 22Nov 19, 2024
Syndromic X-linked intellectual disability 145Nov 19, 2024
Syndromic X-linked intellectual disability 342Nov 19, 2024
Syndromic X-linked intellectual disability 943Nov 19, 2024
Syndromic X-linked intellectual disability Claes-Jensen type10Nov 19, 2024
Syndromic X-linked intellectual disability Najm type4Nov 19, 2024
Syndromic X-linked intellectual disability Nascimento type2Jul 18, 2024
Syndromic X-linked intellectual disability Raymond type2Nov 19, 2024
Syndromic X-linked intellectual disability Siderius type3Nov 19, 2024
Syndromic X-linked intellectual disability Snyder type1Jul 18, 2024
Syndromic disease6Nov 19, 2024
Syndromic intellectual disability2Nov 19, 2024
Syndromic microphthalmia type 51Dec 21, 2022
Synpolydactyly type 21Nov 19, 2024
TARP syndrome7Nov 19, 2024
TCF12-related craniosynostosis4Nov 19, 2024
TELO2-related intellectual disability-neurodevelopmental disorder2Jul 18, 2024
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome4Jul 18, 2024
TNF receptor-associated periodic fever syndrome (TRAPS)1Dec 21, 2022
TTN-related myopathy11Nov 19, 2024
TUBB3-related tubulinopathy1Nov 19, 2024
TWIST1-related craniosynostosis1Jul 18, 2024
Tatton-Brown-Rahman overgrowth syndrome9Nov 19, 2024
Tay-Sachs disease9Jul 18, 2024
Tay-Sachs disease, variant AB1Jul 18, 2024
Teebi hypertelorism syndrome 11Nov 19, 2024
Telangiectasia, hereditary hemorrhagic, type 117Nov 19, 2024
Telangiectasia, hereditary hemorrhagic, type 210Nov 19, 2024
Temple-Baraitser syndrome1Jul 18, 2024
Tenorio syndrome1Dec 21, 2022
Tessadori-van Haaften neurodevelopmental syndrome 12Jul 18, 2024
Testicular anomalies with or without congenital heart disease3Jul 18, 2024
Testosterone 17-beta-dehydrogenase deficiency3Jul 18, 2024
Tetralogy of Fallot2Dec 21, 2022
Thanatophoric dysplasia type 11Nov 19, 2024
Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies1Nov 19, 2024
Thrombocytopenia 23Jul 18, 2024
Thrombocytopenia 52Jul 18, 2024
Thrombocytopenia 8, with dysmorphic features and developmental delay1Nov 19, 2024
Thrombocytopenia, X-linked, with or without dyserythropoietic anemia1Nov 19, 2024
Thrombophilia due to protein C deficiency, autosomal dominant3Nov 19, 2024
Thrombophilia due to protein C deficiency, autosomal recessive1Nov 19, 2024
Thrombophilia due to protein S deficiency, autosomal dominant1Nov 19, 2024
Thrombophilia due to thrombin defect3Nov 19, 2024
Thyroglobulin synthesis defect1Dec 21, 2022
Thyroid dyshormonogenesis 62Nov 19, 2024
Thyroid hormone resistance syndrome2Nov 19, 2024
Thyroid hormone resistance, generalized, autosomal dominant2Nov 19, 2024
Timothy syndrome4Jul 18, 2024
Timothy syndrome type 11Jul 18, 2024
Tolchin-Le Caignec syndrome2Jul 18, 2024
Tooth agenesis, selective, 31Jul 18, 2024
Tooth agenesis, selective, 43Nov 19, 2024
Tooth agenesis, selective, 71Dec 21, 2022
Tooth agenesis, selective, X-linked, 11Nov 19, 2024
Torsion dystonia 62Jul 18, 2024
Townes-Brocks syndrome 14Nov 19, 2024
Treacher Collins syndrome 17Jul 18, 2024
Treacher Collins syndrome 41Dec 21, 2022
Trichohepatoenteric syndrome 14Nov 19, 2024
Trichohepatoenteric syndrome 21Dec 21, 2022
Trichorhinophalangeal dysplasia type I3Jul 18, 2024
Trichorhinophalangeal syndrome type I or III2Aug 3, 2022
Trimethylaminuria1Jul 18, 2024
Tuberous sclerosis 17Nov 19, 2024
Tuberous sclerosis 214Nov 19, 2024
Tumor predisposition syndrome 22Jul 18, 2024
Tumoral calcinosis, hyperphosphatemic, familial, 12Jul 18, 2024
Type 2 collagenopathy6Nov 19, 2024
Type II complement component 8 deficiency1Nov 19, 2024
Tyrosinase-negative oculocutaneous albinism4Nov 19, 2024
Tyrosinase-positive oculocutaneous albinism10Nov 19, 2024
Tyrosinemia type I1Jul 18, 2024
Tyrosinemia type III1Nov 19, 2024
Ullrich congenital muscular dystrophy 1A3Nov 19, 2024
Ullrich congenital muscular dystrophy 24Nov 19, 2024
Upshaw-Schulman syndrome4Nov 19, 2024
Usher syndrome2Nov 19, 2024
Usher syndrome type 13Nov 19, 2024
Usher syndrome type 1C4Nov 19, 2024
Usher syndrome type 1D8Nov 19, 2024
Usher syndrome type 2A23Nov 19, 2024
Usher syndrome type 2C5Nov 19, 2024
Usmani-Riazuddin syndrome, autosomal dominant2Nov 19, 2024
VEXAS syndrome1Jul 18, 2024
Van Maldergem syndrome 12Nov 19, 2024
Van Maldergem syndrome 27Jul 18, 2024
Vanishing white matter disease8Dec 21, 2022
Variegate porphyria4Nov 19, 2024
Vasculitis due to ADA2 deficiency3Jul 18, 2024
Ventriculomegaly and arthrogryposis1Nov 19, 2024
Ventriculomegaly-cystic kidney disease2Jul 18, 2024
Vertebral, cardiac, renal, and limb defects syndrome 31Jul 18, 2024
Ververi-Brady syndrome4Jul 18, 2024
Very long chain acyl-CoA dehydrogenase deficiency5Jul 18, 2024
Visceral myopathy 14Nov 19, 2024
Vissers-Bodmer syndrome5Nov 19, 2024
Vitelliform macular dystrophy 22Nov 19, 2024
Waardenburg syndrome1Nov 19, 2024
Waardenburg syndrome type 14Nov 19, 2024
Waardenburg syndrome type 2A3Nov 19, 2024
Waardenburg syndrome type 4A2Nov 19, 2024
Wagner syndrome2Jul 18, 2024
Warburg micro syndrome 22Dec 21, 2022
Warburg-cinotti syndrome1Nov 19, 2024
Warsaw breakage syndrome5Nov 19, 2024
Weaver syndrome3Nov 19, 2024
Weill-Marchesani syndrome 11Jul 18, 2024
Weiss-Kruszka syndrome7Nov 19, 2024
Wieacker-Wolff syndrome3Nov 19, 2024
Wieacker-Wolff syndrome, female-restricted1Nov 19, 2024
Wiedemann-Steiner syndrome28Nov 19, 2024
Wilson disease13Nov 19, 2024
Wilson-Turner syndrome4Nov 19, 2024
Wiskott-Aldrich syndrome2Jul 18, 2024
Wolff-Parkinson-White pattern1Jul 18, 2024
Wolfram syndrome 115Nov 19, 2024
X-linked Alport syndrome61Nov 19, 2024
X-linked Emery-Dreifuss muscular dystrophy1Dec 21, 2022
X-linked Opitz G/BBB syndrome2Nov 19, 2024
X-linked agammaglobulinemia3Nov 19, 2024
X-linked central congenital hypothyroidism with late-onset testicular enlargement2Nov 19, 2024
X-linked chondrodysplasia punctata 12Dec 21, 2022
X-linked complex neurodevelopmental disorder2Nov 19, 2024
X-linked complicated corpus callosum dysgenesis1Jul 18, 2024
X-linked cone-rod dystrophy 32Nov 19, 2024
X-linked distal spinal muscular atrophy type 31Nov 19, 2024
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia1Nov 19, 2024
X-linked hydrocephalus syndrome6Nov 19, 2024
X-linked intellectual disability1Jul 18, 2024
X-linked intellectual disability Cabezas type5Nov 19, 2024
X-linked intellectual disability with marfanoid habitus1Dec 21, 2022
X-linked intellectual disability, Cantagrel type3Nov 19, 2024
X-linked intellectual disability, Stocco dos Santos type1Nov 19, 2024
X-linked intellectual disability, van Esch type3Nov 19, 2024
X-linked intellectual disability-cerebellar hypoplasia syndrome1Jul 18, 2024
X-linked intellectual disability-psychosis-macroorchidism syndrome3Nov 19, 2024
X-linked intellectual disability-short stature-overweight syndrome2Jul 18, 2024
X-linked lymphoproliferative disease due to SH2D1A deficiency1Nov 19, 2024
X-linked lymphoproliferative disease due to XIAP deficiency1Nov 19, 2024
X-linked mixed hearing loss with perilymphatic gusher2Nov 19, 2024
X-linked myopathy with excessive autophagy1Nov 19, 2024
X-linked myopathy with postural muscle atrophy2Nov 19, 2024
X-linked recessive nephrolithiasis with renal failure1Dec 21, 2022
X-linked severe combined immunodeficiency2Nov 19, 2024
X-linked severe congenital neutropenia1Jul 18, 2024
X-linked sideroblastic anemia 12Nov 19, 2024
X-linked syndromic intellectual disability1Jul 18, 2024
Xeroderma pigmentosum group A2Dec 21, 2022
Xeroderma pigmentosum group B3Jul 18, 2024
Xeroderma pigmentosum, group D2Nov 19, 2024
ZTTK syndrome13Nov 19, 2024
Zimmermann-Laband syndrome 22Nov 19, 2024
Zinc deficiency, transient neonatal1Dec 21, 2022
alpha Thalassemia1Nov 19, 2024
beta Thalassemia1Nov 19, 2024
not specified3Apr 4, 2023
von Willebrand disease type 15Nov 19, 2024
von Willebrand disease type 22Nov 19, 2024