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Al Jalila Children’s Genomics Center (Al Jalila Childrens Speciality Hospital)

General information

Al Jalila Children’s Genomics Center
Al Jalila Childrens Speciality Hospital
Dubai
United Arab Emirates - 0000

Organization ID: 507199

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 1701

Gene

GeneSubmissionsLast Updated
A2ML12Dec 17, 2022
AARS11Dec 17, 2022
ABCA123Nov 10, 2024
ABCA21Oct 4, 2021
ABCA415Nov 10, 2024
ABCB112Oct 4, 2021
ABCB61Oct 4, 2021
ABCG22Dec 17, 2022
ABCG81Nov 10, 2024
ACADM2Nov 10, 2024
ACAN2Nov 10, 2024
ACAT11Nov 10, 2024
ACO21Nov 10, 2024
ACOX21Oct 4, 2021
ACP51Oct 4, 2021
ACTB2Nov 10, 2024
ADAM171Oct 4, 2021
ADAMTSL11Oct 4, 2021
ADAMTSL41Oct 4, 2021
ADAT31Nov 10, 2024
ADD31Nov 10, 2024
ADGRE22Oct 4, 2021
ADGRV15Oct 4, 2021
ADNP1Oct 4, 2021
AFG2A1Oct 4, 2021
AGA1Nov 10, 2024
AGBL21Oct 4, 2021
AGBL52Nov 10, 2024
AGMO1Oct 4, 2021
AGR21Nov 10, 2024
AGXT1Nov 10, 2024
AHDC11Oct 4, 2021
AHI11Oct 4, 2021
AIRE2Nov 10, 2024
AKAP91Oct 4, 2021
AKR1D11Nov 10, 2024
ALDH18A12Nov 10, 2024
ALDH1A31Nov 10, 2024
ALDH1A3-AS11Nov 10, 2024
ALDH3A21Nov 10, 2024
ALDH7A13Nov 10, 2024
ALG132Nov 10, 2024
ALG91Oct 4, 2021
ALMS12Nov 10, 2024
ALOX12B1Oct 4, 2021
ALPI1Dec 17, 2022
ALPL1Nov 10, 2024
AMPD12Oct 4, 2021
AMPD21Nov 10, 2024
ANK12Nov 10, 2024
ANK31Oct 4, 2021
ANKRD114Nov 10, 2024
ANKRD261Oct 4, 2021
ANKRD371Nov 10, 2024
ANO51Dec 17, 2022
ANTXR21Nov 10, 2024
AOX11Oct 4, 2021
AP1G11Nov 10, 2024
AP1S21Nov 10, 2024
AP1S32Oct 4, 2021
AP4B11Oct 4, 2021
AP4B1-AS11Oct 4, 2021
AP4E11Nov 10, 2024
AP4S11Nov 10, 2024
APC2Nov 10, 2024
APOL11Oct 4, 2021
AQP21Nov 10, 2024
AQP5-AS11Nov 10, 2024
ARAP31Oct 4, 2021
ARHGEF101Oct 4, 2021
ARHGEF181Oct 4, 2021
ARHGEF91Oct 4, 2021
ARID1B5Nov 10, 2024
ARID21Oct 4, 2021
ARPC1B1Oct 4, 2021
ARSA2Nov 10, 2024
ARSB3Nov 10, 2024
ASAH11Nov 10, 2024
ASH1L1Nov 10, 2024
ASL1Nov 10, 2024
ASNS2Nov 10, 2024
ASPM2Nov 10, 2024
ASPN1Oct 4, 2021
ASS11Nov 10, 2024
ASXL33Nov 10, 2024
ATAD3A1Oct 4, 2021
ATIC1Oct 4, 2021
ATM5Nov 10, 2024
ATN11Oct 4, 2021
ATP13A21Oct 4, 2021
ATP1A21Dec 17, 2022
ATP1A32Nov 10, 2024
ATP8A21Oct 4, 2021
ATP8B14Dec 17, 2022
ATP8B1-AS12Dec 17, 2022
ATP9A2Nov 10, 2024
ATRX1Nov 10, 2024
ATXN21Oct 4, 2021
ATXN71Dec 17, 2022
AUH1Nov 10, 2024
AVIL1Nov 10, 2024
AVPR21Oct 4, 2021
B3GALNT21Nov 10, 2024
B3GAT31Nov 10, 2024
BBS101Dec 17, 2022
BBS121Nov 10, 2024
BBS21Nov 10, 2024
BCHE1Nov 10, 2024
BCL11A1Nov 10, 2024
BCR1Oct 4, 2021
BCS1L1Nov 10, 2024
BEST12Nov 10, 2024
BFSP11Oct 4, 2021
BIRC61Dec 17, 2022
BIVM-ERCC51Nov 10, 2024
BLTP12Oct 4, 2021
BMPR21Nov 10, 2024
BPTF1Oct 4, 2021
BRAF2Nov 10, 2024
BRPF11Nov 10, 2024
BSCL21Nov 10, 2024
BTD8Nov 10, 2024
C11orf652Dec 17, 2022
C12orf571Nov 10, 2024
C2CD31Oct 4, 2021
C32Dec 17, 2022
C4B1Nov 16, 2020
C91Oct 4, 2021
CA21Nov 10, 2024
CACNA1A1Oct 4, 2021
CACNA1C2Dec 17, 2022
CACNA1D2Dec 17, 2022
CACNA1S1Oct 4, 2021
CANT11Nov 10, 2024
CAPN32Dec 17, 2022
CARMIL21Dec 17, 2022
CASK1Nov 10, 2024
CASP101Oct 4, 2021
CASQ22Oct 4, 2021
CAST1Nov 10, 2024
CAV11Oct 4, 2021
CC2D2A4Nov 10, 2024
CCDC401Oct 4, 2021
CCDC88C1Oct 4, 2021
CCDST2Oct 4, 2021
CCN61Nov 16, 2020
CCNO3Nov 10, 2024
CD1631Nov 15, 2021
CD2472Dec 17, 2022
CD2AP1Dec 17, 2022
CD2BP2-DT1Oct 4, 2021
CD362Nov 10, 2024
CD3D1Dec 17, 2022
CD40LG1Dec 17, 2022
CD841Nov 15, 2021
CDH231Nov 10, 2024
CDH32Nov 10, 2024
CDHR11Oct 4, 2021
CDK101Oct 4, 2021
CDK131Nov 10, 2024
CDKL52Nov 10, 2024
CDKN1C2Nov 10, 2024
CEL2Nov 10, 2024
CENPP1Oct 4, 2021
CEP1042Oct 4, 2021
CEP1201Oct 4, 2021
CEP1641Oct 4, 2021
CEP191Oct 4, 2021
CEP2904Nov 10, 2024
CERS11Oct 4, 2021
CERS31Nov 10, 2024
CFH1Oct 4, 2021
CFHR51Oct 4, 2021
CFL21Oct 4, 2021
CFTR16Nov 10, 2024
CFTR-AS13Nov 10, 2024
CHAT1Oct 4, 2021
CHD31Oct 4, 2021
CHD77Nov 10, 2024
CHIT11Oct 4, 2021
CHRNA11Dec 17, 2022
CHRNA42Dec 17, 2022
CHRNA71Oct 4, 2021
CHRNB11Nov 10, 2024
CHRND1Oct 4, 2021
CHRNE1Dec 17, 2022
CHRNG1Nov 10, 2024
CIC1Oct 4, 2021
CIT1Nov 10, 2024
CLCNKB1Nov 10, 2024
CLDN142Dec 17, 2022
CLDN14-AS12Dec 17, 2022
CLDN161Oct 4, 2021
CLDN192Nov 10, 2024
CLN61Oct 4, 2021
CLN81Oct 4, 2021
CLRN11Oct 4, 2021
CNGA35Nov 10, 2024
CNGB32Nov 10, 2024
CNOT11Nov 10, 2024
COG61Nov 10, 2024
COL11A11Oct 4, 2021
COL11A23Nov 10, 2024
COL18A12Nov 10, 2024
COL1A11Nov 10, 2024
COL1A21Dec 17, 2022
COL27A11Nov 10, 2024
COL4A12Nov 10, 2024
COL4A33Dec 17, 2022
COL4A61Oct 4, 2021
COL5A11Oct 4, 2021
COL6A12Oct 4, 2021
COL6A23Nov 10, 2024
COL6A37Dec 17, 2022
COL7A12Nov 10, 2024
COL9A22Nov 10, 2024
COPA1Oct 4, 2021
COQ61Oct 4, 2021
COQ8A2Oct 4, 2021
COQ8B1Oct 4, 2021
COQ91Oct 4, 2021
CPLANE11Dec 17, 2022
CPS14Nov 10, 2024
CPT21Dec 17, 2022
CRB15Nov 10, 2024
CREBBP2Nov 10, 2024
CRYBA41Oct 4, 2021
CRYBB11Oct 4, 2021
CSF3R1Dec 17, 2022
CSNK2A11Nov 10, 2024
CSNK2B1Nov 10, 2024
CSPP13Nov 10, 2024
CTCF2Nov 10, 2024
CTNNA31Oct 4, 2021
CTNNB11Nov 10, 2024
CTNS3Nov 10, 2024
CTNS-AS12Nov 10, 2024
CTRC1Dec 17, 2022
CTSK1Nov 10, 2024
CTU21Nov 10, 2024
CUL73Nov 10, 2024
CWC271Oct 4, 2021
CYBB1Dec 17, 2022
CYP17A11Nov 10, 2024
CYP1B13Nov 10, 2024
CYP21A23Nov 10, 2024
CYP2B62Oct 4, 2021
CYP4V21Oct 4, 2021
CZ1P-ASNS2Nov 10, 2024
DARS22Oct 4, 2021
DBT1Nov 10, 2024
DCDC21Oct 4, 2021
DCLRE1C1Oct 4, 2021
DDB11Nov 10, 2024
DEPDC55Nov 10, 2024
DGAT13Nov 10, 2024
DGUOK1Nov 10, 2024
DGUOK-AS11Nov 10, 2024
DHCR71Oct 4, 2021
DHODH1Oct 4, 2021
DIAPH12Nov 10, 2024
DKC12Dec 17, 2022
DLD1Nov 10, 2024
DLL11Nov 10, 2024
DLX61Oct 4, 2021
DLX6-AS11Oct 4, 2021
DMAC2L2Oct 4, 2021
DMD3Nov 10, 2024
DMGDH3Dec 17, 2022
DMXL21Oct 4, 2021
DNAH13Dec 17, 2022
DNAH113Nov 10, 2024
DNAH52Oct 4, 2021
DNAJB21Dec 17, 2022
DNASE1L31Nov 10, 2024
DNHD11Oct 4, 2021
DNM21Oct 4, 2021
DOCK22Dec 17, 2022
DOCK61Nov 10, 2024
DOCK83Dec 17, 2022
DOK11Nov 10, 2024
DOK73Nov 10, 2024
DONSON3Nov 10, 2024
DSC22Oct 4, 2021
DSE2Oct 4, 2021
DST3Oct 4, 2021
DUOX25Dec 17, 2022
DUSP291Nov 10, 2024
DYNC1H12Nov 10, 2024
DYNC2H12Oct 4, 2021
DYRK1A1Nov 10, 2024
DYSF3Dec 17, 2022
ECEL11Nov 10, 2024
EDA1Dec 17, 2022
EDARADD1Nov 10, 2024
EFCAB13-DT1Nov 10, 2024
EFL11Oct 4, 2021
EHMT12Nov 10, 2024
EIF2AK32Nov 10, 2024
EIF2B21Oct 4, 2021
ELMOD31Oct 4, 2021
EMC101Nov 10, 2024
ENPP12Oct 4, 2021
EP3001Oct 4, 2021
EP4001Oct 4, 2021
EPB41L12Dec 17, 2022
EPG52Nov 10, 2024
EPM2A1Dec 17, 2022
EPM2A-DT1Dec 17, 2022
EPS81Oct 4, 2021
ERCC11Oct 4, 2021
ERCC51Nov 10, 2024
ERCC62Oct 4, 2021
ESPN1Oct 4, 2021
ETFDH2Nov 10, 2024
ETHE12Nov 10, 2024
EVC22Nov 10, 2024
EXOC71Nov 10, 2024
EXOSC92Nov 10, 2024
EXT13Nov 10, 2024
EXT21Oct 4, 2021
EYA12Dec 17, 2022
EYS3Oct 4, 2021
F22Nov 10, 2024
F51Oct 4, 2021
FAH2Nov 10, 2024
FAM161B1Oct 4, 2021
FANCA1Oct 4, 2021
FANCC2Nov 10, 2024
FANCD22Oct 4, 2021
FAT22Dec 17, 2022
FBN13Nov 10, 2024
FBP11Nov 10, 2024
FBP21Oct 4, 2021
FBXL43Nov 10, 2024
FBXO222Nov 10, 2024
FBXO71Oct 4, 2021
FBXW71Nov 10, 2024
FDFT11Oct 4, 2021
FERMT11Oct 4, 2021
FERMT31Nov 10, 2024
FERRY31Oct 4, 2021
FGA1Oct 4, 2021
FGD12Nov 10, 2024
FGF122Dec 17, 2022
FGFR13Nov 10, 2024
FGFR22Oct 4, 2021
FGFR36Nov 10, 2024
FH1Oct 4, 2021
FIBP1Nov 10, 2024
FKBP102Nov 10, 2024
FKRP1Oct 4, 2021
FLG2Oct 4, 2021
FLNA1Oct 4, 2021
FLNB3Nov 10, 2024
FLNC2Nov 10, 2024
FN11Oct 4, 2021
FOXC12Oct 4, 2021
FOXE11Oct 4, 2021
FOXG12Nov 10, 2024
FOXL21Nov 10, 2024
FOXP11Nov 10, 2024
FOXP21Dec 17, 2022
FRRS1L1Dec 17, 2022
FUCA11Nov 10, 2024
FZD21Nov 10, 2024
G6PC11Dec 17, 2022
G6PD1Dec 17, 2022
GAA5Nov 10, 2024
GABBR21Oct 4, 2021
GABRA11Nov 10, 2024
GABRB22Nov 10, 2024
GABRB32Nov 10, 2024
GALC1Nov 10, 2024
GALE1Dec 17, 2022
GALNS2Nov 10, 2024
GALNT31Nov 10, 2024
GALT2Nov 10, 2024
GAMT1Nov 10, 2024
GATA32Nov 10, 2024
GATA41Oct 4, 2021
GATAD11Oct 4, 2021
GBE11Oct 4, 2021
GBF11Oct 4, 2021
GCK1Nov 10, 2024
GDF11Oct 4, 2021
GFAP1Dec 17, 2022
GFRA11Nov 10, 2024
GH-LCR3Dec 17, 2022
GHR1Dec 17, 2022
GHSR1Dec 17, 2022
GIGYF21Oct 4, 2021
GIPC31Oct 4, 2021
GJB27Nov 10, 2024
GJB41Oct 4, 2021
GLA2Nov 10, 2024
GLB14Nov 10, 2024
GLDC2Nov 10, 2024
GLI31Oct 4, 2021
GLMN1Dec 17, 2022
GNAO11Nov 10, 2024
GNAS2Dec 7, 2024
GNAT11Oct 4, 2021
GNAT21Nov 10, 2024
GNE1Oct 4, 2021
GNG12-AS11Nov 10, 2024
GNPTAB3Nov 10, 2024
GPHN1Dec 17, 2022
GPI1Oct 4, 2021
GPIHBP11Oct 4, 2021
GPR1793Oct 4, 2021
GPSM21Oct 4, 2021
GRIN2A2Nov 10, 2024
GRIN2B4Nov 10, 2024
GTPBP32Nov 10, 2024
GYG21Oct 4, 2021
HACD12Nov 10, 2024
HBB7Dec 17, 2022
HECW22Nov 10, 2024
HEXA1Nov 10, 2024
HEXB1Nov 10, 2024
HGD1Nov 10, 2024
HGSNAT2Nov 10, 2024
HHAT1Oct 4, 2021
HIVEP21Nov 10, 2024
HNF1A1Dec 17, 2022
HNRNPUL2-BSCL21Nov 10, 2024
HOXA111Dec 17, 2022
HOXA31Oct 4, 2021
HPS31Nov 10, 2024
HPS41Oct 4, 2021
HSALR11Oct 4, 2021
HSD11B21Nov 10, 2024
HSD17B43Nov 10, 2024
HSD3B71Nov 10, 2024
HSPG24Oct 4, 2021
HTT1Oct 4, 2021
HYDIN2Oct 4, 2021
IBA571Nov 10, 2024
IDS2Oct 4, 2021
IDUA2Oct 4, 2021
IFI27L11Feb 2, 2023
IFI443Feb 2, 2023
IFI44L1Nov 15, 2021
IFIH114Nov 15, 2024
IFNA101Feb 2, 2023
IFNA141Feb 2, 2023
IFNA211Nov 15, 2021
IFNA41Nov 15, 2021
IFNA61Nov 15, 2021
IFNAR12Feb 2, 2023
IFNAR24Feb 2, 2023
IFNAR2-IL10RB4Feb 2, 2023
IFNB11Nov 15, 2021
IFNGR22Feb 2, 2023
IFNL21Feb 2, 2023
IFRD21Oct 4, 2021
IFT431Oct 4, 2021
IGFBP71Nov 10, 2024
IGHMBP21Dec 17, 2022
IKBKB1Nov 10, 2024
IKBKE2Dec 17, 2022
IKZF11Nov 10, 2024
IL17RB1Oct 4, 2021
IL17RC1Oct 4, 2021
IL1RN2Oct 4, 2021
IL22RA21Nov 15, 2021
IL2RG1Nov 10, 2024
IL6ST2Oct 4, 2021
ILDR11Oct 4, 2021
IMPDH11Nov 10, 2024
INF21Oct 4, 2021
INPP5E3Nov 10, 2024
INPPL12Nov 10, 2024
INS1Nov 10, 2024
INSR1Nov 10, 2024
INTS12Oct 4, 2021
IQCB11Dec 17, 2022
IRAK32Feb 2, 2023
IRF31Nov 15, 2021
IRF61Oct 4, 2021
IRF71Oct 4, 2021
ITFG21Nov 10, 2024
ITGA61Nov 10, 2024
ITGA71Oct 4, 2021
ITGB32Nov 10, 2024
IVD4Nov 10, 2024
JAG11Nov 10, 2024
JAM31Nov 10, 2024
JMJD1C1Dec 17, 2022
KANK11Oct 4, 2021
KANSL11Oct 4, 2021
KAT6A2Nov 10, 2024
KAT6B1Nov 10, 2024
KCNB11Dec 17, 2022
KCNC11Oct 4, 2021
KCNJ11Nov 10, 2024
KCNJ101Oct 4, 2021
KCNJ112Nov 10, 2024
KCNMA11Oct 4, 2021
KCNMA1-AS11Oct 4, 2021
KCNQ11Oct 4, 2021
KCNQ24Nov 10, 2024
KCNV22Nov 10, 2024
KDM6B2Nov 10, 2024
KIAA05861Oct 4, 2021
KIF141Nov 10, 2024
KIF1C2Dec 17, 2022
KIF5C1Nov 10, 2024
KIF72Oct 4, 2021
KIRREL11Oct 4, 2021
KLHL71Nov 10, 2024
KMT2A3Nov 10, 2024
KMT2B1Nov 10, 2024
KMT2C4Nov 10, 2024
KMT2D6Nov 10, 2024
KMT2E1Nov 10, 2024
KRT181Oct 4, 2021
KRT81Oct 4, 2021
KRTAP10-121Oct 4, 2021
KRTAP10-31Oct 4, 2021
L2HGDH3Oct 4, 2021
LAMA24Dec 17, 2022
LAMB22Oct 4, 2021
LAMB33Nov 10, 2024
LAMC21Oct 4, 2021
LAMC33Oct 4, 2021
LAMP21Oct 4, 2021
LARGE13Dec 17, 2022
LARP71Nov 10, 2024
LARS24Oct 4, 2021
LCA51Nov 10, 2024
LDB31Oct 4, 2021
LDHAL6B1Oct 4, 2021
LDLR1Nov 10, 2024
LDLRAD21Oct 4, 2021
LFNG1Oct 4, 2021
LHFPL51Nov 10, 2024
LIFR1Nov 10, 2024
LINS11Nov 10, 2024
LIPA1Oct 4, 2021
LMNA3Nov 10, 2024
LOC1019297101Nov 10, 2024
LOC1027240581Nov 10, 2024
LOC1053714681Nov 15, 2021
LOC1053715662Oct 4, 2021
LOC1060293121Dec 17, 2022
LOC1060501022Oct 4, 2021
LOC1060964161Oct 4, 2021
LOC1060990627Dec 17, 2022
LOC1065017131Nov 10, 2024
LOC1067808003Nov 10, 2024
LOC1071262811Dec 17, 2022
LOC1071335107Dec 17, 2022
LOC1073033382Oct 4, 2021
LOC1094614841Oct 4, 2021
LOC1096115891Oct 4, 2021
LOC1100063191Oct 4, 2021
LOC1116744721Oct 4, 2021
LOC1116744751Nov 10, 2024
LOC1118119651Nov 10, 2024
LOC1125336711Oct 4, 2021
LOC1125774861Oct 4, 2021
LOC1136338771Nov 10, 2024
LOC1215875741Nov 10, 2024
LOC1217250461Oct 4, 2021
LOC1217406382Dec 17, 2022
LOC1235228031Oct 4, 2021
LOC1239562722Oct 4, 2021
LOC1254677681Nov 10, 2024
LOC1268056122Dec 17, 2022
LOC1268057931Nov 10, 2024
LOC1268057941Nov 10, 2024
LOC1268058221Nov 10, 2024
LOC1268062521Nov 10, 2024
LOC1268064261Oct 4, 2021
LOC1268596903Nov 10, 2024
LOC1268598371Oct 4, 2021
LOC1268611101Nov 10, 2024
LOC1268622649Dec 7, 2024
LOC1268624471Oct 4, 2021
LOC1268624841Oct 4, 2021
LOC1268631451Oct 4, 2021
LOC1268632561Nov 10, 2024
LOC1299290271Oct 4, 2021
LOC1299310831Oct 4, 2021
LOC1299361431Oct 4, 2021
LOC1299367881Oct 4, 2021
LOC1299373391Oct 4, 2021
LOC1299922961Oct 4, 2021
LOC1299936901Dec 17, 2022
LOC1299938953Nov 10, 2024
LOC1299941261Oct 4, 2021
LOC1299945261Dec 17, 2022
LOC1299951441Oct 4, 2021
LOC1299970341Oct 4, 2021
LOC1299973811Dec 17, 2022
LOC1299979281Oct 4, 2021
LOC1300031351Nov 10, 2024
LOC1300055981Oct 4, 2021
LOC1300077001Oct 4, 2021
LOC1300087911Oct 4, 2021
LOC1300598921Nov 10, 2024
LOC1300613701Oct 4, 2021
LOC1300625681Oct 4, 2021
LOC1300629451Nov 10, 2024
LOC1300662991Oct 4, 2021
LORICRIN1Nov 10, 2024
LOXHD16Nov 10, 2024
LOXL32Nov 10, 2024
LPAR61Oct 4, 2021
LPIN22Dec 17, 2022
LRBA2Oct 4, 2021
LRIT31Oct 4, 2021
LRP21Nov 10, 2024
LRP41Dec 17, 2022
LRP4-AS11Dec 17, 2022
LRP52Oct 4, 2021
LRP61Dec 17, 2022
LRRC511Oct 4, 2021
LRRK11Nov 10, 2024
LRRK21Oct 4, 2021
LRTOMT1Oct 4, 2021
LTBP21Oct 4, 2021
LTBP42Oct 4, 2021
LY91Nov 15, 2021
LYST6Nov 10, 2024
MACF13Dec 17, 2022
MALT11Oct 4, 2021
MAN2B13Nov 10, 2024
MAN2B21Oct 4, 2021
MAP2K21Dec 17, 2022
MAPK11Dec 17, 2022
MAST11Nov 10, 2024
MBD51Dec 17, 2022
MBTPS11Oct 4, 2021
MC4R2Nov 10, 2024
MCCC21Nov 10, 2024
MCIDAS1Nov 10, 2024
MCOLN11Oct 4, 2021
MECP24Nov 10, 2024
MED13L2Nov 10, 2024
MEFV16Dec 7, 2024
MEGF101Nov 10, 2024
MEIS22Nov 10, 2024
MEN11Nov 10, 2024
MERTK2Nov 10, 2024
MET1Nov 10, 2024
METTL232Nov 10, 2024
MFF-DT3Dec 17, 2022
MICU12Nov 10, 2024
MID21Oct 4, 2021
MIPEP2Nov 10, 2024
MIR302CHG1Nov 10, 2024
MIR4733HG1Nov 10, 2024
MIR68481Dec 17, 2022
MLH11Oct 4, 2021
MMAB1Nov 10, 2024
MMACHC1Nov 10, 2024
MMP151Nov 10, 2024
MMP21Oct 4, 2021
MMP91Oct 4, 2021
MMUT3Nov 10, 2024
MPDZ1Oct 4, 2021
MPL1Oct 4, 2021
MPV171Dec 17, 2022
MPZL21Oct 4, 2021
MRE111Oct 4, 2021
MSC-AS11Oct 4, 2021
MSRB31Oct 4, 2021
MTCL11Oct 4, 2021
MUC5B1Nov 10, 2024
MVD1Oct 4, 2021
MVK4Nov 10, 2024
MVP-DT3Nov 10, 2024
MYBPC21Oct 4, 2021
MYBPC34Nov 10, 2024
MYH111Nov 10, 2024
MYH141Oct 4, 2021
MYH7B1Dec 17, 2022
MYH92Nov 10, 2024
MYLK1Dec 17, 2022
MYO15A3Oct 4, 2021
MYO1E1Oct 4, 2021
MYO5A1Oct 4, 2021
MYO5B2Nov 10, 2024
MYO61Oct 4, 2021
MYOCD1Oct 4, 2021
NAGA1Nov 10, 2024
NAGLU1Nov 10, 2024
NALCN2Oct 4, 2021
NANS1Oct 4, 2021
NARS21Oct 4, 2021
NBEA1Nov 10, 2024
NCF11Dec 17, 2022
NCKAP1L2Nov 10, 2024
NDUFB41Oct 4, 2021
NEB5Dec 17, 2022
NEDD4L2Oct 4, 2021
NELL12Oct 4, 2021
NEXMIF1Nov 10, 2024
NF128Nov 10, 2024
NFAT51Dec 17, 2022
NFIB1Nov 10, 2024
NFKB21Dec 17, 2022
NGF1Nov 10, 2024
NGF-AS11Nov 10, 2024
NGLY11Oct 4, 2021
NKX2-11Oct 4, 2021
NKX6-21Nov 10, 2024
NLRC41Oct 4, 2021
NLRP13Oct 4, 2021
NLRP125Dec 17, 2022
NLRP21Nov 15, 2021
NME31Oct 4, 2021
NME81Oct 4, 2021
NNT1Dec 17, 2022
NOD24Dec 17, 2022
NOTCH22Oct 4, 2021
NOTCH31Nov 10, 2024
NPC15Oct 4, 2021
NPC21Nov 10, 2024
NPHP11Oct 4, 2021
NPHP41Oct 4, 2021
NPHS14Nov 10, 2024
NPHS21Oct 4, 2021
NPR21Oct 4, 2021
NR2E32Nov 10, 2024
NRL2Dec 17, 2022
NRXN12Dec 17, 2022
NSD13Nov 10, 2024
NSUN21Nov 10, 2024
NTRK11Nov 10, 2024
NUP931Oct 4, 2021
NUTM2B2Oct 4, 2021
NUTM2B-AS12Oct 4, 2021
OCLN2Nov 10, 2024
OFD12Nov 10, 2024
OPA12Nov 10, 2024
OPHN11Oct 4, 2021
ORAI11Nov 10, 2024
ORC12Oct 4, 2021
OSBPL21Oct 4, 2021
OTOA1Oct 4, 2021
OTOF1Oct 4, 2021
OTOG5Dec 17, 2022
OXCT11Nov 10, 2024
P3H21Nov 10, 2024
PACS11Nov 10, 2024
PACS22Nov 10, 2024
PAH7Nov 10, 2024
PAK31Nov 10, 2024
PALB21Nov 10, 2024
PANK21Nov 10, 2024
PARS22Dec 17, 2022
PAX22Nov 10, 2024
PAX31Nov 10, 2024
PCARE2Nov 10, 2024
PCAT71Oct 4, 2021
PCCA2Nov 10, 2024
PCCB1Nov 10, 2024
PCDH151Oct 4, 2021
PCDH192Nov 10, 2024
PCNT1Oct 4, 2021
PCSK11Nov 10, 2024
PDE6A1Nov 10, 2024
PDHA12Nov 10, 2024
PDHX1Oct 4, 2021
PDILT1Oct 4, 2021
PDZD71Nov 10, 2024
PDZD81Nov 10, 2024
PEX12Oct 4, 2021
PEX121Nov 10, 2024
PEX161Nov 10, 2024
PEX261Oct 4, 2021
PEX64Nov 10, 2024
PGAP31Nov 10, 2024
PGBD31Oct 4, 2021
PGK11Oct 4, 2021
PGM11Nov 10, 2024
PGM31Dec 17, 2022
PHF21A1Oct 4, 2021
PHF31Oct 4, 2021
PHF61Nov 10, 2024
PHGDH1Nov 10, 2024
PHKA11Oct 4, 2021
PHKA21Oct 4, 2021
PHKG21Oct 4, 2021
PHYH1Oct 4, 2021
PIDD11Nov 10, 2024
PIEZO12Nov 15, 2024
PIGT1Oct 4, 2021
PIK3CA1Nov 10, 2024
PIK3CD4Dec 17, 2022
PITX31Oct 4, 2021
PJVK1Nov 10, 2024
PKD17Nov 10, 2024
PKD1L11Oct 4, 2021
PKHD18Nov 10, 2024
PKP22Nov 10, 2024
PLCB11Oct 4, 2021
PLCB31Nov 10, 2024
PLCE11Dec 17, 2022
PLCG22Dec 17, 2022
PLEC6Oct 4, 2021
PLOD12Nov 10, 2024
PMM21Oct 4, 2021
PMS21Dec 17, 2022
PNKP1Oct 4, 2021
PNPO4Nov 10, 2024
POGZ1Oct 4, 2021
POLD13Nov 10, 2024
POLG2Nov 10, 2024
POLGARF2Nov 10, 2024
POLR1C1Nov 10, 2024
POLR3B1Nov 10, 2024
POMT11Dec 17, 2022
PPP1R211Nov 10, 2024
PQBP11Nov 10, 2024
PRDM51Oct 4, 2021
PRF11Nov 10, 2024
PRG42Nov 10, 2024
PRICKLE12Oct 4, 2021
PRKN1Nov 10, 2024
PRMT71Oct 4, 2021
PROC2Nov 10, 2024
PRODH1Oct 4, 2021
PRPH21Nov 10, 2024
PRRT23Nov 10, 2024
PRSS11Dec 17, 2022
PRSS81Oct 4, 2021
PRX1Nov 10, 2024
PSAP1Nov 10, 2024
PSMB82Dec 17, 2022
PSMD121Nov 10, 2024
PTBP21Oct 4, 2021
PTEN3Nov 10, 2024
PTPN112Nov 10, 2024
PTPN231Oct 4, 2021
PTRH21Dec 17, 2022
PYCR22Nov 10, 2024
PYGM2Nov 10, 2024
PYY1Oct 4, 2021
QARS11Nov 10, 2024
RAB231Nov 10, 2024
RAB27A1Nov 15, 2021
RAC11Oct 4, 2021
RAC21Oct 4, 2021
RAD211Nov 10, 2024
RAI11Dec 17, 2022
RANGAP11Oct 4, 2021
RARS12Nov 10, 2024
RARS21Oct 4, 2021
RB11Oct 4, 2021
RBP31Dec 17, 2022
RDH121Dec 17, 2022
RDX1Oct 4, 2021
RECQL41Nov 10, 2024
RELN3Dec 17, 2022
RET2Oct 4, 2021
RFX61Nov 10, 2024
RHOBTB21Dec 17, 2022
RIF11Dec 17, 2022
RIT12Nov 10, 2024
RLBP12Dec 17, 2022
RNASEH2A1Nov 10, 2024
RNASEH2C1Nov 10, 2024
RNF131Nov 10, 2024
ROBO31Nov 10, 2024
ROR22Oct 4, 2021
RORB1Nov 10, 2024
RP1L11Oct 4, 2021
RPE652Nov 10, 2024
RPGRIP12Nov 10, 2024
RPGRIP1L1Nov 10, 2024
RPL36A-HNRNPH22Nov 10, 2024
RRP81Oct 4, 2021
RS14Nov 10, 2024
RSPH31Oct 4, 2021
RSPH4A1Nov 10, 2024
RSPH91Nov 10, 2024
RUNX22Nov 10, 2024
RYR16Nov 10, 2024
RYR22Oct 4, 2021
RYR31Oct 4, 2021
S100A61Oct 4, 2021
S1PR21Oct 4, 2021
SACS1Oct 4, 2021
SALL13Oct 4, 2021
SALL41Oct 4, 2021
SAMD111Oct 4, 2021
SAMD92Dec 17, 2022
SAMHD11Oct 4, 2021
SATB21Nov 10, 2024
SBF12Nov 10, 2024
SCAMP41Nov 10, 2024
SCN10A1Dec 17, 2022
SCN1A2Nov 10, 2024
SCN1A-AS11Oct 4, 2021
SCN3A3Nov 10, 2024
SCN4A4Nov 10, 2024
SCN5A1Oct 4, 2021
SCN8A1Nov 10, 2024
SCN9A1Oct 4, 2021
SCNN1A1Dec 17, 2022
SCNN1G1Nov 10, 2024
SCRIB1Oct 4, 2021
SDHA1Oct 4, 2021
SELENON1Oct 4, 2021
SERPINA11Oct 4, 2021
SERPINA31Oct 4, 2021
SERPINA61Oct 4, 2021
SERPINB61Oct 4, 2021
SERPINB81Nov 10, 2024
SERPINC11Oct 4, 2021
SERPINF11Nov 10, 2024
SERPING11Nov 10, 2024
SETD21Oct 4, 2021
SETD52Nov 10, 2024
SETX3Dec 17, 2022
SFTA31Oct 4, 2021
SFTPB1Dec 17, 2022
SGCA3Nov 10, 2024
SGCB2Dec 17, 2022
SGCD1Nov 10, 2024
SGSH1Nov 10, 2024
SH2D1A1Nov 10, 2024
SH3BP21Oct 4, 2021
SH3PXD2B1Oct 4, 2021
SH3TC21Oct 4, 2021
SHH1Nov 10, 2024
SHOC21Oct 4, 2021
SHROOM31Oct 4, 2021
SHROOM3-AS11Oct 4, 2021
SIGMAR11Dec 17, 2022
SIK12Dec 17, 2022
SIL11Nov 10, 2024
SIN3A1Oct 4, 2021
SIX11Oct 4, 2021
SKIC21Oct 4, 2021
SKIC32Oct 4, 2021
SLC12A21Dec 17, 2022
SLC12A35Nov 10, 2024
SLC12A61Nov 10, 2024
SLC13A51Oct 4, 2021
SLC22A121Oct 4, 2021
SLC22A181Oct 4, 2021
SLC22A18AS1Oct 4, 2021
SLC22A51Nov 10, 2024
SLC25A201Nov 10, 2024
SLC25A241Oct 4, 2021
SLC26A12Oct 4, 2021
SLC26A32Nov 10, 2024
SLC26A49Nov 10, 2024
SLC34A11Nov 10, 2024
SLC38A81Oct 4, 2021
SLC39A141Nov 10, 2024
SLC3A11Nov 10, 2024
SLC45A11Nov 10, 2024
SLC5A11Dec 17, 2022
SLC5A71Nov 10, 2024
SLC7A71Nov 10, 2024
SLITRK61Oct 4, 2021
SLURP11Nov 10, 2024
SLX42Oct 4, 2021
SMAD41Nov 10, 2024
SMAD71Oct 4, 2021
SMARCA11Dec 17, 2022
SMARCA41Oct 4, 2021
SMARCB11Nov 10, 2024
SMC1A1Nov 10, 2024
SMCHD11Oct 4, 2021
SMPD12Nov 10, 2024
SNHG142Nov 10, 2024
SNX102Nov 10, 2024
SNX141Nov 10, 2024
SOAT21Oct 4, 2021
SOHLH11Oct 4, 2021
SON1Dec 17, 2022
SOS11Nov 10, 2024
SOX52Nov 10, 2024
SPAG11Oct 4, 2021
SPAG171Oct 4, 2021
SPART3Nov 10, 2024
SPAST2Nov 10, 2024
SPATA71Nov 10, 2024
SPG114Nov 10, 2024
SPINK52Nov 10, 2024
SPINT21Dec 17, 2022
SPRY11Oct 4, 2021
SPTA12Nov 10, 2024
SPTAN15Dec 17, 2022
SPTB1Nov 10, 2024
SQSTM11Nov 10, 2024
SRA11Oct 4, 2021
SRCAP1Nov 10, 2024
SRD5A32Nov 10, 2024
SSH12Oct 4, 2021
ST141Nov 10, 2024
ST3GAL31Oct 4, 2021
STAC31Nov 10, 2024
STAT11Nov 10, 2024
STAT23Feb 2, 2023
STAT31Nov 10, 2024
STAT5B1Nov 10, 2024
STIL1Dec 17, 2022
STING11Oct 4, 2021
STRC1Oct 4, 2021
STX1B1Nov 10, 2024
STXBP13Nov 10, 2024
STXBP31Oct 4, 2021
SUMF12Nov 10, 2024
SUOX1Nov 10, 2024
SVBP1Nov 10, 2024
SYN12Nov 10, 2024
SYNE110Dec 17, 2022
SYNJ12Nov 10, 2024
TALDO11Nov 10, 2024
TANC21Nov 10, 2024
TANGO22Nov 10, 2024
TAOK11Nov 10, 2024
TAPT11Oct 4, 2021
TBC1D10B1Oct 4, 2021
TBC1D242Oct 4, 2021
TBC1D8B2Oct 4, 2021
TBCEL-TECTA1Oct 4, 2021
TBCK1Oct 4, 2021
TBK11Feb 2, 2023
TBL1XR11Oct 4, 2021
TCF121Oct 4, 2021
TCF42Nov 10, 2024
TCN21Dec 17, 2022
TDRD91Oct 4, 2021
TECTA1Oct 4, 2021
TENT5A1Oct 4, 2021
TERT1Oct 4, 2021
TEX141Oct 4, 2021
TFAP2A2Dec 17, 2022
TFAP2A-AS22Dec 17, 2022
TFE31Nov 10, 2024
TGFB22Oct 4, 2021
TGFBR21Nov 10, 2024
THG1L1Oct 4, 2021
TICAM12Feb 2, 2023
TICRR1Oct 4, 2021
TINF21Oct 4, 2021
TK21Nov 10, 2024
TLDC21Oct 4, 2021
TLK22Nov 10, 2024
TLR31Nov 15, 2021
TLR41Feb 2, 2023
TLR62Feb 2, 2023
TMC12Nov 10, 2024
TMEM1382Nov 10, 2024
TMEM2401Dec 17, 2022
TMEM50B1Feb 2, 2023
TMEM674Nov 10, 2024
TMEM941Nov 10, 2024
TMPRSS62Dec 17, 2022
TNFAIP31Nov 16, 2020
TNFRSF13B3Dec 17, 2022
TNFRSF1A2Nov 10, 2024
TNNT11Oct 4, 2021
TNXB3Nov 10, 2024
TOM12Dec 17, 2022
TOR1AIP11Oct 4, 2021
TPI11Nov 10, 2024
TPM21Nov 10, 2024
TPO4Nov 10, 2024
TRAF31Nov 15, 2021
TRAP12Oct 4, 2021
TRAPPC113Nov 10, 2024
TRAPPC121Dec 17, 2022
TRAPPC21Nov 10, 2024
TRB1Dec 17, 2022
TRIM141Oct 4, 2021
TRIM691Nov 15, 2021
TRIO3Nov 10, 2024
TRIOBP5Oct 4, 2021
TRIP121Nov 10, 2024
TRPA11Oct 4, 2021
TRPM12Nov 10, 2024
TRPM61Nov 10, 2024
TRPM71Oct 4, 2021
TSC11Oct 4, 2021
TSC28Nov 10, 2024
TSEN541Oct 4, 2021
TSPEAR3Oct 4, 2021
TSPOAP12Oct 4, 2021
TSPYL11Oct 4, 2021
TTC21B1Oct 4, 2021
TTC7A1Oct 4, 2021
TTI11Oct 4, 2021
TTN11Nov 10, 2024
TTN-AS13Oct 4, 2021
TTR1Nov 10, 2024
TUBB2B1Oct 4, 2021
TUBB4A1Nov 10, 2024
TXNRD21Dec 17, 2022
UBE3A2Nov 10, 2024
UBQLN41Oct 4, 2021
UFSP21Nov 10, 2024
UGP21Nov 10, 2024
UGT1A5Dec 7, 2024
UGT1A15Dec 7, 2024
UGT1A105Dec 7, 2024
UGT1A35Dec 7, 2024
UGT1A45Dec 7, 2024
UGT1A55Dec 7, 2024
UGT1A65Dec 7, 2024
UGT1A75Dec 7, 2024
UGT1A85Dec 7, 2024
UGT1A95Dec 7, 2024
UNC13D4Dec 17, 2022
UNC45B1Oct 4, 2021
UNG1Oct 4, 2021
UPB11Oct 4, 2021
UROC11Nov 10, 2024
USH2A2Oct 4, 2021
USP71Nov 10, 2024
USP9X1Oct 4, 2021
VANGL12Oct 4, 2021
VARS21Oct 4, 2021
VCAN1Oct 4, 2021
VCAN-AS11Oct 4, 2021
VCP1Oct 4, 2021
VDR2Nov 10, 2024
VIPAS391Oct 4, 2021
VLDLR1Nov 10, 2024
VPS111Oct 4, 2021
VPS13B2Nov 10, 2024
VPS26C1Nov 10, 2024
VWF3Nov 10, 2024
WAC1Nov 10, 2024
WAS1Dec 17, 2022
WASHC41Nov 10, 2024
WDR452Nov 10, 2024
WDR45B1Nov 10, 2024
WDR813Nov 10, 2024
WFS11Oct 4, 2021
WHRN1Oct 4, 2021
WLS1Nov 10, 2024
WWOX3Nov 10, 2024
XPA1Nov 10, 2024
XYLT12Nov 10, 2024
ZBTB181Oct 4, 2021
ZEB21Nov 10, 2024
ZFYVE264Oct 4, 2021
ZFYVE271Dec 17, 2022
ZIC51Oct 4, 2021
ZMPSTE241Nov 10, 2024
ZNF1412Oct 4, 2021
ZNF2761Oct 4, 2021
ZNF2921Oct 4, 2021
ZNF3351Oct 4, 2021
ZNF4621Oct 4, 2021
ZNF4691Oct 4, 2021
ZNF6271Oct 4, 2021
ZNF6681Nov 10, 2024
ZNF6991Nov 10, 2024
ZPBP1Oct 4, 2021

Condition

NameSubmissionsLast Updated
3-Methylglutaconic aciduria1Nov 10, 2024
3-Methylglutaconic aciduria type 31Nov 10, 2024
3-methylcrotonyl-CoA carboxylase 2 deficiency1Nov 10, 2024
3M syndrome 13Nov 10, 2024
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder1Oct 4, 2021
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome1Oct 4, 2021
ALG9 congenital disorder of glycosylation1Oct 4, 2021
Abnormal heart morphology1Nov 10, 2024
Achromatopsia 25Nov 10, 2024
Achromatopsia 32Nov 10, 2024
Achromatopsia 41Nov 10, 2024
Acroerythrokeratoderma1Nov 10, 2024
Acromesomelic dysplasia 1, Maroteaux type1Oct 4, 2021
Adams-Oliver syndrome 21Nov 10, 2024
Agenesis of the corpus callosum with peripheral neuropathy1Nov 10, 2024
Aicardi-Goutieres syndrome 31Nov 10, 2024
Aicardi-Goutieres syndrome 41Nov 10, 2024
Aicardi-Goutieres syndrome 75Nov 15, 2024
Al Kaissi syndrome1Oct 4, 2021
Alagille syndrome due to a NOTCH2 point mutation2Oct 4, 2021
Alkaptonuria1Nov 10, 2024
Alkuraya-Kucinskas syndrome2Oct 4, 2021
Alpha-1-antitrypsin deficiency1Oct 4, 2021
Alpha-N-acetylgalactosaminidase deficiency type 11Nov 10, 2024
Alpha-thalassemia/intellectual disability syndrome1Nov 10, 2024
Alstrom syndrome1Nov 10, 2024
Alternating hemiplegia of childhood 21Nov 10, 2024
Amyloidosis1Nov 10, 2024
Anemia1Nov 10, 2024
Angelman syndrome2Nov 10, 2024
Angioedema1Nov 10, 2024
Anterior segment dysgenesis 11Oct 4, 2021
Apparent mineralocorticoid excess1Nov 10, 2024
Argininosuccinate lyase deficiency1Nov 10, 2024
Arrhythmogenic right ventricular dysplasia 112Oct 4, 2021
Arrhythmogenic right ventricular dysplasia 131Oct 4, 2021
Arrhythmogenic right ventricular dysplasia 91Nov 10, 2024
Arthrogryposis2Nov 10, 2024
Arthrogryposis, renal dysfunction, and cholestasis 21Oct 4, 2021
Aspartylglucosaminuria1Nov 10, 2024
Asphyxiating thoracic dystrophy 32Oct 4, 2021
Ataxia-telangiectasia syndrome2Nov 10, 2024
Ataxia-telangiectasia-like disorder 11Oct 4, 2021
Atypical hemolytic-uremic syndrome with C3 anomaly1Oct 4, 2021
Autoimmune connective tissue disease and vasculitis1Nov 23, 2020
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome1Nov 10, 2024
Autoinflammatory syndrome, familial, Behcet-like1Nov 16, 2020
Autosomal dominant Parkinson disease 81Oct 4, 2021
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome1Oct 4, 2021
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome1Nov 10, 2024
Autosomal dominant nocturnal frontal lobe epilepsy 11Oct 4, 2021
Autosomal dominant nonsyndromic hearing loss 11Oct 4, 2021
Autosomal dominant nonsyndromic hearing loss 121Oct 4, 2021
Autosomal dominant nonsyndromic hearing loss 231Oct 4, 2021
Autosomal dominant nonsyndromic hearing loss 4A1Oct 4, 2021
Autosomal dominant omodysplasia1Nov 10, 2024
Autosomal dominant optic atrophy classic form1Oct 4, 2021
Autosomal recessive Robinow syndrome2Oct 4, 2021
Autosomal recessive ataxia due to ubiquinone deficiency2Oct 4, 2021
Autosomal recessive ataxia, Beauce type1Oct 4, 2021
Autosomal recessive congenital ichthyosis 21Oct 4, 2021
Autosomal recessive inherited pseudoxanthoma elasticum1Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2B2Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2D1Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2E1Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2Q3Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2Y1Oct 4, 2021
Autosomal recessive limb-girdle muscular dystrophy type R182Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 1021Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 151Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 161Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 1A2Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 221Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 241Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 285Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 291Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 33Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 421Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 631Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 681Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 741Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 773Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 91Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 911Oct 4, 2021
Autosomal recessive nonsyndromic hearing loss 983Oct 4, 2021
Autosomal recessive spastic paraplegia type 781Oct 4, 2021
Autosomal recessive spinocerebellar ataxia 121Oct 4, 2021
Autosomal systemic lupus erythematosus type 161Nov 10, 2024
Bailey-Bloch congenital myopathy1Nov 10, 2024
Baller-Gerold syndrome1Nov 10, 2024
Bamforth-Lazarus syndrome1Oct 4, 2021
Baraitser-Winter syndrome 12Nov 10, 2024
Bardet-Biedl syndrome 121Nov 10, 2024
Bartter syndrome2Nov 10, 2024
Becker muscular dystrophy1Nov 10, 2024
Bethlem myopathy 1A1Nov 10, 2024
Bietti crystalline corneoretinal dystrophy1Oct 4, 2021
Bifunctional peroxisomal enzyme deficiency1Nov 10, 2024
Biotinidase deficiency8Nov 10, 2024
Blepharophimosis1Nov 10, 2024
Blepharophimosis - intellectual disability syndrome, SBBYS type1Nov 10, 2024
Borjeson-Forssman-Lehmann syndrome1Nov 10, 2024
Brain-lung-thyroid syndrome1Oct 4, 2021
Branchial cleft anomaly6Nov 10, 2024
Branchiooculofacial syndrome1Oct 4, 2021
Branchiootorenal syndrome 11Oct 4, 2021
Brittle cornea syndrome 11Oct 4, 2021
Brittle cornea syndrome 21Oct 4, 2021
Bronchiectasis with or without elevated sweat chloride 31Nov 10, 2024
Brugada syndrome 31Oct 4, 2021
CFHR5 deficiency1Oct 4, 2021
CLOVES syndrome1Nov 10, 2024
COACH syndrome 21Nov 10, 2024
Café-au-lait macules with pulmonary stenosis25Nov 10, 2024
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome2Nov 10, 2024
Candidiasis, familial, 91Oct 4, 2021
Cardiac anomalies - developmental delay - facial dysmorphism syndrome1Nov 10, 2024
Cardiomyopathy3Nov 10, 2024
Carnitine acylcarnitine translocase deficiency1Nov 10, 2024
Carnitine deficiency1Nov 10, 2024
Carpenter syndrome1Nov 10, 2024
Cataract 17 multiple types1Oct 4, 2021
Cataract 331Oct 4, 2021
Cerebellar ataxia1Nov 10, 2024
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 41Oct 4, 2021
Cerebellar hypoplasia1Nov 10, 2024
Cerebral palsy1Nov 10, 2024
Cerebrooculofacioskeletal syndrome 41Oct 4, 2021
Ceroid lipofuscinosis, neuronal, 6B (Kufs type)1Oct 4, 2021
Charcot-Marie-Tooth disease5Nov 10, 2024
Charcot-Marie-Tooth disease type 4B31Oct 4, 2021
Charlevoix-Saguenay spastic ataxia1Oct 4, 2021
Chitotriosidase deficiency1Oct 4, 2021
Chromosome 2q32-q33 deletion syndrome1Nov 10, 2024
Chronic myelogenous leukemia, BCR-ABL1 positive1Oct 4, 2021
Chédiak-Higashi syndrome5Nov 10, 2024
Ciliary dyskinesia, primary, 371Oct 4, 2021
Citrullinemia1Nov 10, 2024
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency3Nov 10, 2024
Cleft palate2Nov 10, 2024
Coffin-Siris syndrome1Nov 10, 2024
Coffin-Siris syndrome 15Nov 10, 2024
Coffin-Siris syndrome 61Oct 4, 2021
Cohen syndrome2Nov 10, 2024
Colorectal cancer1Nov 10, 2024
Colorectal cancer, susceptibility to, 101Oct 4, 2021
Combined PSAP deficiency1Nov 10, 2024
Combined immunodeficiency1Nov 10, 2024
Combined immunodeficiency due to DOCK8 deficiency2Oct 4, 2021
Combined immunodeficiency due to LRBA deficiency2Oct 4, 2021
Combined immunodeficiency due to MALT1 deficiency1Oct 4, 2021
Combined immunodeficiency due to ORAI1 deficiency1Nov 10, 2024
Combined oxidative phosphorylation defect type 232Nov 10, 2024
Complement component 4b deficiency1Nov 16, 2020
Complement component 9 deficiency1Oct 4, 2021
Complex lethal osteochondrodysplasia1Oct 4, 2021
Cone dystrophy with supernormal rod response2Nov 10, 2024
Cone-rod dystrophy 131Nov 10, 2024
Cone-rod dystrophy 151Oct 4, 2021
Congenital bile acid synthesis defect2Nov 10, 2024
Congenital bile acid synthesis defect 61Oct 4, 2021
Congenital diarrhea 7 with exudative enteropathy1Oct 4, 2021
Congenital disorder of deglycosylation1Oct 4, 2021
Congenital disorder of glycosylation1Nov 10, 2024
Congenital heart defects, multiple types, 61Oct 4, 2021
Congenital hyperammonemia, type I3Nov 10, 2024
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome2Nov 10, 2024
Congenital microvillous atrophy2Nov 10, 2024
Congenital multicore myopathy with external ophthalmoplegia2Nov 10, 2024
Congenital muscular dystrophy due to integrin alpha-7 deficiency1Oct 4, 2021
Congenital muscular hypertrophy-cerebral syndrome1Nov 10, 2024
Congenital myasthenic syndrome 2C1Nov 10, 2024
Congenital myopathy 111Nov 10, 2024
Congenital myopathy with fiber type disproportion1Oct 4, 2021
Congenital secretory diarrhea, chloride type2Nov 10, 2024
Congenital stationary night blindness 1C1Oct 4, 2021
Congenital stationary night blindness 1E3Oct 4, 2021
Congenital stationary night blindness 1F1Oct 4, 2021
Congenital stationary night blindness autosomal dominant 31Oct 4, 2021
Conjugate gaze palsy1Nov 10, 2024
Convulsions1Nov 10, 2024
Cornelia de Lange syndrome 41Nov 10, 2024
Cortical dysplasia1Nov 10, 2024
Corticosteroid-binding globulin deficiency1Oct 4, 2021
Crigler-Najjar syndrome1Nov 10, 2024
Crigler-Najjar syndrome type 11Dec 7, 2024
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies2Oct 4, 2021
Cystic fibrosis9Nov 10, 2024
Cystinosis2Nov 10, 2024
Cystinuria1Nov 10, 2024
DEGCAGS syndrome1Nov 10, 2024
DOCK2 deficiency1Oct 4, 2021
Dalmatian hypouricemia1Oct 4, 2021
DeSanto-Shinawi syndrome1Nov 10, 2024
Deafness17Nov 10, 2024
Deficiency of acetyl-CoA acetyltransferase1Nov 10, 2024
Deficiency of beta-ureidopropionase1Oct 4, 2021
Deficiency of butyrylcholinesterase1Nov 10, 2024
Deficiency of fructose-bisphosphatase1Nov 10, 2024
Deficiency of guanidinoacetate methyltransferase1Nov 10, 2024
Deficiency of iodide peroxidase4Nov 10, 2024
Deficiency of steroid 17-alpha-monooxygenase1Nov 10, 2024
Deficiency of transaldolase1Nov 10, 2024
Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema1Nov 15, 2024
Desbuquois dysplasia 11Nov 10, 2024
Desbuquois dysplasia 21Nov 10, 2024
Developmental and epileptic encephalopathy 6B2Nov 10, 2024
Developmental and epileptic encephalopathy 921Nov 10, 2024
Developmental and epileptic encephalopathy, 121Oct 4, 2021
Developmental and epileptic encephalopathy, 151Oct 4, 2021
Developmental and epileptic encephalopathy, 171Nov 10, 2024
Developmental and epileptic encephalopathy, 21Nov 10, 2024
Developmental and epileptic encephalopathy, 251Oct 4, 2021
Developmental and epileptic encephalopathy, 273Nov 10, 2024
Developmental and epileptic encephalopathy, 361Nov 10, 2024
Developmental and epileptic encephalopathy, 42Nov 10, 2024
Developmental and epileptic encephalopathy, 421Oct 4, 2021
Developmental and epileptic encephalopathy, 471Oct 4, 2021
Developmental and epileptic encephalopathy, 621Oct 4, 2021
Developmental and epileptic encephalopathy, 661Nov 10, 2024
Developmental and epileptic encephalopathy, 74Nov 10, 2024
Developmental and epileptic encephalopathy, 731Nov 10, 2024
Developmental and epileptic encephalopathy, 81Oct 4, 2021
Developmental and epileptic encephalopathy, 831Nov 10, 2024
Developmental and epileptic encephalopathy, 92Nov 10, 2024
Developmental delay2Nov 10, 2024
Developmental delay with or without intellectual impairment or behavioral abnormalities1Nov 10, 2024
Developmental disorder1Nov 10, 2024
Developmental dysplasia of the hip1Nov 10, 2024
Diabetes1Nov 10, 2024
Diabetes insipidus1Nov 10, 2024
Diabetes mellitus1Nov 10, 2024
Diarrhea1Nov 10, 2024
Dias-Logan syndrome1Nov 10, 2024
Dimethylglycine dehydrogenase deficiency2Oct 4, 2021
Donnai-Barrow syndrome1Nov 10, 2024
Duane-radial ray syndrome1Oct 4, 2021
Dyskeratosis congenita, X-linked1Oct 4, 2021
EAST syndrome1Oct 4, 2021
Early-onset Parkinson disease 201Nov 10, 2024
Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant1Nov 10, 2024
Ectopia lentis et pupillae1Oct 4, 2021
Ehlers-Danlos syndrome1Nov 10, 2024
Ehlers-Danlos syndrome due to tenascin-X deficiency1Oct 4, 2021
Ehlers-Danlos syndrome, classic type, 11Oct 4, 2021
Ehlers-Danlos syndrome, kyphoscoliotic type 11Oct 4, 2021
Ehlers-Danlos syndrome, musculocontractural type 22Oct 4, 2021
Elliptocytosis 21Oct 4, 2021
Ellis-van Creveld syndrome2Nov 10, 2024
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome1Oct 4, 2021
Epidermolysis bullosa3Nov 10, 2024
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency2Oct 4, 2021
Epidermolysis bullosa simplex 5C, with pyloric atresia1Oct 4, 2021
Epilepsy13Nov 10, 2024
Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders1Oct 4, 2021
Epilepsy, familial focal, with variable foci 12Oct 4, 2021
Epilepsy, progressive myoclonic, 1B2Oct 4, 2021
Epiphyseal dysplasia1Nov 10, 2024
Esophageal squamous cell carcinoma2Nov 10, 2024
Ethylmalonic encephalopathy2Nov 10, 2024
Exostoses1Nov 10, 2024
Exudative vitreoretinopathy 71Nov 10, 2024
Fabry disease2Nov 10, 2024
Familial Mediterranean fever3Dec 7, 2024
Familial Mediterranean fever, autosomal dominant11Dec 7, 2024
Familial cold autoinflammatory syndrome 22Oct 4, 2021
Familial hemophagocytic lymphohistiocytosis1Nov 10, 2024
Familial hemophagocytic lymphohistiocytosis 31Oct 4, 2021
Familial hypokalemia-hypomagnesemia4Nov 10, 2024
Familial infantile myasthenia1Oct 4, 2021
Familial retinal arterial macroaneurysm1Nov 10, 2024
Familial visceral amyloidosis, Ostertag type1Oct 4, 2021
Fanconi anemia1Nov 10, 2024
Fanconi anemia complementation group A1Oct 4, 2021
Fanconi anemia complementation group C1Oct 4, 2021
Fanconi anemia complementation group P2Oct 4, 2021
Fanconi renotubular syndrome 21Nov 10, 2024
Fetal akinesia deformation sequence 32Nov 10, 2024
Fibrous dysplasia of jaw1Oct 4, 2021
Finnish congenital nephrotic syndrome2Oct 4, 2021
Focal segmental glomerulosclerosis 4, susceptibility to1Oct 4, 2021
Focal segmental glomerulosclerosis 61Oct 4, 2021
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome1Oct 4, 2021
Frank-Ter Haar syndrome1Oct 4, 2021
Fucosidosis1Nov 10, 2024
GM1 gangliosidosis4Nov 10, 2024
GNE myopathy1Oct 4, 2021
GRACILE syndrome1Nov 10, 2024
Galactosemia2Nov 10, 2024
Galactosylceramide beta-galactosidase deficiency1Nov 10, 2024
Geleophysic dysplasia 23Nov 10, 2024
Generalized dominant dystrophic epidermolysis bullosa1Oct 4, 2021
Generalized epilepsy1Nov 10, 2024
Gilbert syndrome2Oct 4, 2021
Glanzmann thrombasthenia 22Nov 10, 2024
Glaucoma 3A1Nov 10, 2024
Glioma3Nov 10, 2024
Glomerular sclerosis1Nov 10, 2024
Glomerulopathy with fibronectin deposits 21Oct 4, 2021
Glutaric acidemia IIc2Nov 10, 2024
Glycine encephalopathy2Nov 10, 2024
Glycogen storage disease IXa11Oct 4, 2021
Glycogen storage disease IXc1Oct 4, 2021
Glycogen storage disease IXd1Oct 4, 2021
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1Oct 4, 2021
Glycogen storage disease, type II5Nov 10, 2024
Glycogen storage disease, type V2Nov 10, 2024
Griscelli syndrome type 11Oct 4, 2021
Growth hormone insensitivity with immune dysregulation 1, autosomal recessive1Nov 10, 2024
Hao-Fountain syndrome1Nov 10, 2024
Harel-Yoon syndrome1Oct 4, 2021
Hb SS disease1Oct 4, 2021
Hearing loss, X-linked 61Oct 4, 2021
Hearing loss, autosomal recessive 1111Oct 4, 2021
Hemolytic anemia due to glucophosphate isomerase deficiency1Oct 4, 2021
Hereditary antithrombin deficiency1Oct 4, 2021
Hereditary palmoplantar keratoderma3Nov 10, 2024
Hereditary spastic paraplegia 111Oct 4, 2021
Hereditary spastic paraplegia 154Oct 4, 2021
Hereditary spastic paraplegia 42Nov 10, 2024
Hereditary spastic paraplegia 471Oct 4, 2021
Hereditary spastic paraplegia 631Nov 10, 2024
Hereditary spastic paraplegia 9A2Nov 10, 2024
Hereditary von Willebrand disease3Nov 10, 2024
Hermansky-Pudlak syndrome 31Nov 10, 2024
Hermansky-Pudlak syndrome 41Oct 4, 2021
Heterotaxy, visceral, 8, autosomal1Oct 4, 2021
Heterotopia, periventricular, X-linked dominant1Oct 4, 2021
High myopia-sensorineural deafness syndrome1Oct 4, 2021
Holoprosencephaly 31Nov 10, 2024
Huntington disease1Oct 4, 2021
Hyaline fibromatosis syndrome1Nov 10, 2024
Hydrocephalus, nonsyndromic, autosomal recessive 21Oct 4, 2021
Hyper-IgE syndrome1Nov 10, 2024
Hyper-IgM syndrome type 51Oct 4, 2021
Hypercholesterolemia, familial, 11Nov 10, 2024
Hyperimmunoglobulin D with periodic fever1Nov 10, 2024
Hyperlipoproteinemia, type 1D1Oct 4, 2021
Hyperostosis cranialis interna1Nov 10, 2024
Hyperoxaluria1Nov 10, 2024
Hyperphenylalaninemia6Nov 10, 2024
Hyperphosphatasia with intellectual disability syndrome 41Nov 10, 2024
Hypertrophic cardiomyopathy 42Oct 4, 2021
Hypogonadotropic hypogonadism 2 with or without anosmia1Nov 10, 2024
Hypogonadotropic hypogonadism 5 with or without anosmia4Nov 10, 2024
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome1Nov 10, 2024
Hypomyelinating leukodystrophy 121Oct 4, 2021
Hypomyelinating leukodystrophy 91Oct 4, 2021
Hypoparathyroidism, deafness, renal disease syndrome1Nov 10, 2024
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome1Nov 10, 2024
Hypotonia, infantile, with psychomotor retardation and characteristic facies 31Oct 4, 2021
Hypotrichosis1Nov 10, 2024
IMAGe syndrome1Nov 10, 2024
Ichthyosis5Nov 10, 2024
Immunodeficiency1Nov 10, 2024
Immunodeficiency 142Oct 4, 2021
Immunodeficiency 251Oct 4, 2021
Immunodeficiency 391Oct 4, 2021
Immunodeficiency 72 with autoinflammation1Nov 10, 2024
Immunodeficiency 953Nov 10, 2024
Immunodeficiency, common variable, 21Oct 4, 2021
Inflammatory bowel disease 13Oct 4, 2021
Inflammatory skin and bowel disease, neonatal, 11Oct 4, 2021
Intellectual developmental disorder with autism and dysmorphic facies1Nov 10, 2024
Intellectual developmental disorder with cardiac defects and dysmorphic facies1Nov 10, 2024
Intellectual developmental disorder with dysmorphic facies and ptosis1Nov 10, 2024
Intellectual developmental disorder with neuropsychiatric features1Nov 10, 2024
Intellectual disability21Nov 10, 2024
Intellectual disability, X-linked 1011Oct 4, 2021
Intellectual disability, autosomal dominant 111Oct 4, 2021
Intellectual disability, autosomal dominant 161Oct 4, 2021
Intellectual disability, autosomal dominant 221Oct 4, 2021
Intellectual disability, autosomal dominant 451Oct 4, 2021
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency1Oct 4, 2021
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome1Oct 4, 2021
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome1Oct 4, 2021
Intellectual disability-severe speech delay-mild dysmorphism syndrome1Nov 10, 2024
Intestinal hypomagnesemia 11Nov 10, 2024
Iron-refractory iron deficiency anemia1Oct 4, 2021
Isovaleryl-CoA dehydrogenase deficiency4Nov 10, 2024
Joubert syndrome 13Nov 10, 2024
Joubert syndrome 162Nov 10, 2024
Joubert syndrome 213Nov 10, 2024
Joubert syndrome 231Oct 4, 2021
Joubert syndrome 252Oct 4, 2021
Joubert syndrome 311Oct 4, 2021
Joubert syndrome 71Nov 10, 2024
Joubert syndrome 92Oct 4, 2021
Junctional epidermolysis bullosa, non-Herlitz type2Oct 4, 2021
Juvenile retinoschisis1Oct 4, 2021
KBG syndrome3Nov 10, 2024
Kahrizi syndrome2Nov 10, 2024
Kindler syndrome1Oct 4, 2021
Kleefstra syndrome 12Nov 10, 2024
Kleefstra syndrome 23Nov 10, 2024
Knobloch syndrome2Nov 10, 2024
Koolen-de Vries syndrome1Oct 4, 2021
L-2-hydroxyglutaric aciduria3Oct 4, 2021
Lamb-Shaffer syndrome2Nov 10, 2024
Larsen syndrome1Nov 10, 2024
Lateral meningocele syndrome1Nov 10, 2024
Leber congenital amaurosis 104Nov 10, 2024
Leber congenital amaurosis 31Nov 10, 2024
Leber congenital amaurosis 51Nov 10, 2024
Leber congenital amaurosis 61Oct 4, 2021
Leber congenital amaurosis 83Nov 10, 2024
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome2Nov 10, 2024
Leukocyte adhesion deficiency1Nov 10, 2024
Leukodystrophy4Nov 10, 2024
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome2Oct 4, 2021
Lipodystrophy1Nov 10, 2024
Lissencephaly 9 with complex brainstem malformation1Oct 4, 2021
Loeys-Dietz syndrome 21Nov 10, 2024
Loeys-Dietz syndrome 42Oct 4, 2021
Long QT syndrome 111Oct 4, 2021
Loricrin keratoderma1Nov 10, 2024
Lung adenocarcinoma1Nov 10, 2024
Lymphangiomyomatosis6Nov 10, 2024
Lymphatic malformation 61Oct 4, 2021
Lymphoproliferative disorder1Nov 10, 2024
Lysinuric protein intolerance1Nov 10, 2024
Lysosomal acid lipase deficiency1Oct 4, 2021
MEGF10-related myopathy1Nov 10, 2024
Macrocephaly1Nov 10, 2024
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1Oct 4, 2021
Macular dystrophy3Nov 10, 2024
Majeed syndrome1Oct 4, 2021
Malignant tumor of breast1Nov 10, 2024
Malignant tumor of pancreas1Nov 10, 2024
Mandibular hypoplasia-deafness-progeroid syndrome1Oct 4, 2021
Mandibuloacral dysplasia1Nov 10, 2024
Mandibuloacral dysplasia with type B lipodystrophy1Nov 10, 2024
Mannosidosis, alpha-, types I and II3Nov 10, 2024
Maple syrup urine disease1Nov 10, 2024
Marinesco-Sjögren syndrome1Nov 10, 2024
Maturity onset diabetes mellitus in young1Nov 10, 2024
Maturity-onset diabetes of the young type 21Nov 10, 2024
Maturity-onset diabetes of the young type 81Oct 4, 2021
Medium-chain acyl-coenzyme A dehydrogenase deficiency2Nov 10, 2024
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations1Nov 10, 2024
Megabladder, congenital1Oct 4, 2021
Megacystis-microcolon-intestinal hypoperistalsis syndrome 21Nov 10, 2024
Meier-Gorlin syndrome 12Oct 4, 2021
Melanoma2Nov 10, 2024
Menke-Hennekam syndrome 11Nov 10, 2024
Metachromatic leukodystrophy2Nov 10, 2024
Metaphyseal anadysplasia 21Oct 4, 2021
Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome1Nov 10, 2024
Methylmalonic aciduria3Nov 10, 2024
Methylmalonic aciduria and homocystinuria1Nov 10, 2024
Microcephalic primordial dwarfism due to ZNF335 deficiency1Oct 4, 2021
Microcephalic primordial dwarfism, Alazami type1Nov 10, 2024
Microcephaly5Nov 10, 2024
Microcephaly 17, primary, autosomal recessive1Nov 10, 2024
Microcephaly 20, primary, autosomal recessive1Nov 10, 2024
Microcephaly 5, primary, autosomal recessive2Nov 10, 2024
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome1Oct 4, 2021
Micrognathia1Nov 10, 2024
Microphthalmia1Nov 10, 2024
Miller syndrome1Oct 4, 2021
Mitochondrial DNA depletion syndrome 133Nov 10, 2024
Mitochondrial DNA depletion syndrome 2, myopathic form1Nov 10, 2024
Mowat-Wilson syndrome1Nov 10, 2024
Mucolipidosis type IV1Oct 4, 2021
Mucopolysaccharidosis type 63Nov 10, 2024
Mucopolysaccharidosis, MPS-II2Oct 4, 2021
Mucopolysaccharidosis, MPS-III-A1Nov 10, 2024
Mucopolysaccharidosis, MPS-III-C1Nov 10, 2024
Mucopolysaccharidosis, MPS-IV-A2Nov 10, 2024
Muenke syndrome4Nov 10, 2024
Multicentric osteolysis nodulosis arthropathy spectrum1Oct 4, 2021
Multiple congenital exostosis1Oct 4, 2021
Multiple endocrine neoplasia, type 11Nov 10, 2024
Multiple gastrointestinal atresias1Oct 4, 2021
Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects1Nov 10, 2024
Multiple mitochondrial dysfunctions syndrome 31Nov 10, 2024
Multiple pterygium syndrome1Nov 10, 2024
Multiple sclerosis1Nov 10, 2024
Multiple sulfatase deficiency2Nov 10, 2024
Multisystem inflammatory syndrome in children24Nov 15, 2021
Muscle AMP deaminase deficiency2Oct 4, 2021
Muscular dystrophy5Nov 10, 2024
Muscular dystrophy, limb-girdle, autosomal dominant 41Oct 4, 2021
Muscular dystrophy, limb-girdle, autosomal recessive 231Oct 4, 2021
Muscular dystrophy-dystroglycanopathy1Nov 10, 2024
Muscular dystrophy-dystroglycanopathy type B51Oct 4, 2021
Myoclonus1Nov 10, 2024
Myofibrillar myopathy 41Oct 4, 2021
Myopia1Nov 10, 2024
Myopia 28, autosomal recessive2Nov 10, 2024
Nemaline myopathy 24Oct 4, 2021
Nemaline myopathy 51Oct 4, 2021
Nephronophthisis 111Nov 10, 2024
Nephronophthisis 121Oct 4, 2021
Nephronophthisis 151Oct 4, 2021
Nephropathic cystinosis1Oct 4, 2021
Nephrotic syndrome2Nov 10, 2024
Nephrotic syndrome, type 121Oct 4, 2021
Nephrotic syndrome, type 21Oct 4, 2021
Nephrotic syndrome, type 91Oct 4, 2021
Netherton syndrome2Nov 10, 2024
Neu-Laxova syndrome 11Nov 10, 2024
Neurodegeneration with ataxia1Nov 10, 2024
Neurodegeneration with brain iron accumulation 51Nov 10, 2024
Neurodevelopmental disorder3Nov 10, 2024
Neurodevelopmental disorder with ataxia1Nov 10, 2024
Neurodevelopmental disorder with brain abnormalities1Nov 10, 2024
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities2Nov 10, 2024
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies1Oct 4, 2021
Neurodevelopmental disorder with dysmorphic facies and variable seizures1Nov 10, 2024
Neurodevelopmental disorder with hypotonia2Nov 10, 2024
Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures1Nov 10, 2024
Neurodevelopmental disorder with or without early-onset generalized epilepsy1Nov 10, 2024
Neurodevelopmental disorder with poor growth1Nov 10, 2024
Neurodevelopmental disorder with poor growth and behavioral abnormalities2Nov 10, 2024
Neurodevelopmental disorder with seizures and brain atrophy1Nov 10, 2024
Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures1Nov 10, 2024
Neurofibromatosis, type 11Oct 4, 2021
Neuronopathy, distal hereditary motor, type 7A1Nov 10, 2024
Neutrophil immunodeficiency syndrome1Oct 4, 2021
Niemann-Pick disease, type C15Oct 4, 2021
Night blindness1Nov 10, 2024
Noonan syndrome 12Nov 10, 2024
Noonan syndrome 41Nov 10, 2024
Noonan syndrome 82Nov 10, 2024
Noonan syndrome-like disorder with loose anagen hair 11Oct 4, 2021
O'Donnell-Luria-Rodan syndrome1Nov 10, 2024
Obesity3Nov 10, 2024
Obesity due to CEP19 deficiency1Oct 4, 2021
Occult macular dystrophy1Oct 4, 2021
Oculopharyngeal myopathy with leukoencephalopathy 12Oct 4, 2021
Odontohypophosphatasia1Nov 10, 2024
Okur-Chung neurodevelopmental syndrome1Nov 10, 2024
Opsismodysplasia1Nov 10, 2024
Optic atrophy 91Nov 10, 2024
Osteogenesis imperfecta4Nov 10, 2024
Osteogenesis imperfecta, type 181Oct 4, 2021
Osteopetrosis2Nov 10, 2024
Osteosclerotic metaphyseal dysplasia1Nov 10, 2024
PAIN SENSITIVITY QUANTITATIVE TRAIT LOCUS 11Nov 10, 2024
PMM2-congenital disorder of glycosylation1Oct 4, 2021
Paramyotonia congenita of Von Eulenburg1Nov 10, 2024
Parkinson disease 11, autosomal dominant, susceptibility to1Oct 4, 2021
Parkinsonian-pyramidal syndrome1Oct 4, 2021
Peeling skin syndrome 51Nov 10, 2024
Periodic fever-infantile enterocolitis-autoinflammatory syndrome1Oct 4, 2021
Peripheral neuropathy1Nov 10, 2024
Periventricular nodular heterotopia 72Oct 4, 2021
Peroxisome biogenesis disorder 4B2Nov 10, 2024
Peroxisome biogenesis disorder 8B1Nov 10, 2024
Peroxisome biogenesis disorder type 3B1Nov 10, 2024
Perrault syndrome 12Oct 4, 2021
Perrault syndrome 44Oct 4, 2021
Pettigrew syndrome1Nov 10, 2024
Phenylketonuria1Oct 4, 2021
Pierpont syndrome1Oct 4, 2021
Pierson syndrome1Oct 4, 2021
Pigmentary pallidal degeneration1Nov 10, 2024
Pigmentary retinal dystrophy1Oct 4, 2021
Pitt-Hopkins syndrome2Nov 10, 2024
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease1Oct 4, 2021
Platelet-type bleeding disorder 102Nov 10, 2024
Poirier-Bienvenu neurodevelopmental syndrome1Nov 10, 2024
Polycystic kidney disease 47Nov 10, 2024
Polycystic kidney disease, adult type7Nov 10, 2024
Polyendocrine-polyneuropathy syndrome1Oct 4, 2021
Polyglandular autoimmune syndrome, type 12Nov 10, 2024
Pontocerebellar hypoplasia type 61Oct 4, 2021
Pontocerebellar hypoplasia, type 1D1Sep 17, 2020
Pontoneocerebellar hypoplasia1Nov 10, 2024
Porencephaly-microcephaly-bilateral congenital cataract syndrome1Nov 10, 2024
Porokeratosis 7, multiple types1Oct 4, 2021
Portal hypertension1Nov 10, 2024
Primary ciliary dyskinesia6Nov 10, 2024
Primary ciliary dyskinesia 281Oct 4, 2021
Primary ciliary dyskinesia 291Oct 4, 2021
Primary ciliary dyskinesia 32Oct 4, 2021
Primary ciliary dyskinesia 321Oct 4, 2021
Primary ciliary dyskinesia 52Oct 4, 2021
Primary ciliary dyskinesia 61Oct 4, 2021
Primary ciliary dyskinesia 72Oct 4, 2021
Primary hypomagnesemia1Oct 4, 2021
Progressive familial intrahepatic cholestasis type 22Oct 4, 2021
Progressive myoclonic epilepsy type 71Oct 4, 2021
Progressive pseudorheumatoid dysplasia1Nov 16, 2020
Propionic acidemia3Nov 10, 2024
Proteasome-associated autoinflammatory syndrome 11Oct 4, 2021
Proximal myopathy with extrapyramidal signs1Nov 10, 2024
Pseudo-Hurler polydystrophy1Nov 10, 2024
Pseudo-TORCH syndrome 12Nov 10, 2024
Pseudohypoparathyroidism type I A1Nov 10, 2024
Pseudopseudohypoparathyroidism1Dec 7, 2024
Psoriasis 15, pustular, susceptibility to2Oct 4, 2021
Pulmonary fibrosis1Nov 10, 2024
Pulmonary hypertension1Nov 10, 2024
Pulmonary hypertension, primary, 31Oct 4, 2021
Pyknodysostosis1Nov 10, 2024
Pyridoxal phosphate-responsive seizures4Nov 10, 2024
Pyruvate dehydrogenase E1-alpha deficiency2Nov 10, 2024
Pyruvate dehydrogenase E3 deficiency1Nov 10, 2024
Rabson-Mendenhall syndrome1Nov 10, 2024
Recessive dystrophic epidermolysis bullosa1Nov 10, 2024
Recessive mitochondrial ataxia syndrome1Nov 10, 2024
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome2Nov 10, 2024
Renal cell carcinoma2Nov 10, 2024
Renal hypodysplasia/aplasia 41Nov 10, 2024
Renal hypomagnesemia 5 with ocular involvement2Nov 10, 2024
Renpenning syndrome1Nov 10, 2024
Respiratory infections, recurrent, and failure to thrive with or without diarrhea1Nov 10, 2024
Retinal arteries1Nov 10, 2024
Retinal dystrophy14Nov 10, 2024
Retinitis pigmentosa 101Nov 10, 2024
Retinitis pigmentosa 122Oct 4, 2021
Retinitis pigmentosa 202Nov 10, 2024
Retinitis pigmentosa 253Oct 4, 2021
Retinitis pigmentosa 271Oct 4, 2021
Retinitis pigmentosa 372Nov 10, 2024
Retinitis pigmentosa 382Nov 10, 2024
Retinitis pigmentosa 421Nov 10, 2024
Retinitis pigmentosa 431Nov 10, 2024
Retinitis pigmentosa 542Nov 10, 2024
Retinitis pigmentosa 741Nov 10, 2024
Retinitis pigmentosa 752Nov 10, 2024
Retinitis pigmentosa 811Oct 4, 2021
Retinoschisis2Nov 10, 2024
Rett syndrome5Nov 10, 2024
Rickets1Nov 10, 2024
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency1Oct 4, 2021
STING-associated vasculopathy with onset in infancy1Oct 4, 2021
Sandhoff disease1Nov 10, 2024
Schuurs-Hoeijmakers syndrome1Nov 10, 2024
Severe combined immunodeficiency due to DCLRE1C deficiency1Oct 4, 2021
Severe combined immunodeficiency due to IKK2 deficiency1Nov 10, 2024
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome3Nov 10, 2024
Simpson-Golabi-Behmel syndrome2Nov 10, 2024
Sitosterolemia 11Nov 10, 2024
Sjögren-Larsson syndrome1Nov 10, 2024
Smith-Lemli-Opitz syndrome1Oct 4, 2021
Sotos syndrome3Nov 10, 2024
Spastic Paraplegia 521Nov 10, 2024
Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy1Nov 10, 2024
Spermatogenic failure 231Oct 4, 2021
Spermatogenic failure 301Oct 4, 2021
Spherocytosis3Nov 10, 2024
Sphingomyelin/cholesterol lipidosis2Nov 10, 2024
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome1Nov 10, 2024
Spinocerebellar ataxia 451Oct 4, 2021
Spinocerebellar ataxia type 21Oct 4, 2021
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 22Oct 4, 2021
Spinocerebellar atrophy1Nov 10, 2024
Spondyloenchondrodysplasia with immune dysregulation1Oct 4, 2021
Spondyloepiphyseal dysplasia2Nov 10, 2024
Spondyloepiphyseal dysplasia tarda1Nov 10, 2024
Spondylometaphyseal dysplasia with corneal dystrophy1Nov 10, 2024
Squalene synthase deficiency1Oct 4, 2021
Stankiewicz-Isidor syndrome1Nov 10, 2024
Steel syndrome1Nov 10, 2024
Sterile multifocal osteomyelitis with periostitis and pustulosis1Oct 4, 2021
Stuttering1Nov 10, 2024
Stuve-Wiedemann syndrome1Nov 10, 2024
Succinyl-CoA acetoacetate transferase deficiency1Nov 10, 2024
Sulfite oxidase deficiency1Nov 10, 2024
Susceptibility to severe COVID-1923Feb 2, 2023
TCF12-related craniosynostosis1Oct 4, 2021
TNF receptor-associated periodic fever syndrome (TRAPS)1Nov 16, 2020
Tall stature-intellectual disability-renal anomalies syndrome1Nov 10, 2024
Tay-Sachs disease1Nov 10, 2024
Temtamy syndrome1Nov 10, 2024
Thrombocythemia 21Oct 4, 2021
Thrombocytopenia 21Oct 4, 2021
Thrombophilia 3 due to protein C deficiency2Nov 10, 2024
Thrombophilia due to thrombin defect1Nov 10, 2024
Thyroid dyshormonogenesis 63Oct 4, 2021
Torsion dystonia 41Nov 10, 2024
Trichohepatoenteric syndrome 12Oct 4, 2021
Trichohepatoenteric syndrome 21Oct 4, 2021
Triosephosphate isomerase deficiency1Nov 10, 2024
Troyer syndrome2Nov 10, 2024
Tuberous sclerosis 11Oct 4, 2021
Tumoral calcinosis, hyperphosphatemic, familial, 11Nov 10, 2024
Tyrosinemia2Nov 10, 2024
Urocanate hydratase deficiency1Nov 10, 2024
Usher syndrome1Nov 10, 2024
Usher syndrome type 1D1Oct 4, 2021
Usher syndrome type 2A2Oct 4, 2021
Usher syndrome type 2C2Oct 4, 2021
Usher syndrome type 3A1Oct 4, 2021
Usmani-Riazuddin syndrome, autosomal recessive1Nov 10, 2024
Vanishing white matter disease1Oct 4, 2021
Vibratory urticaria2Oct 4, 2021
Vici syndrome2Nov 10, 2024
Vissers-Bodmer syndrome1Nov 10, 2024
Waardenburg syndrome1Nov 10, 2024
Wagner syndrome1Oct 4, 2021
White-Kernohan syndrome1Nov 10, 2024
Wiedemann-Steiner syndrome2Nov 10, 2024
Wolcott-Rallison dysplasia2Nov 10, 2024
X-linked intellectual disability-cerebellar hypoplasia syndrome1Oct 4, 2021
Xeroderma pigmentosum2Nov 10, 2024
Zaki syndrome1Nov 10, 2024
beta Thalassemia1Oct 4, 2021
not provided213Dec 17, 2022
not specified312Oct 4, 2021

Testing in GTR

Disease nameNumber of tests
ABCD syndrome1 test
Abdominal obesity-metabolic syndrome 31 test
Abetalipoproteinaemia1 test
Achondrogenesis type II1 test
Achondroplasia2 tests
Acquired hemoglobin H disease1 test
Acrodysostosis 1 with or without hormone resistance1 test
Acrodysostosis 2 with or without hormone resistance1 test
Acrofacial dysostosis Cincinnati type1 test
Acromelic frontonasal dysostosis1 test
Acromesomelic dysplasia 31 test
Adams-Oliver syndrome 51 test
Adrenoleukodystrophy1 test
Adult hypophosphatasia1 test
Afibrinogenemia1 test
Agammaglobulinemia 7, autosomal recessive1 test
Age related macular degeneration 11 test
Age related macular degeneration 131 test
Age related macular degeneration 141 test
Aicardi-Goutieres syndrome 21 test
Aicardi-Goutieres syndrome 31 test
Aicardi-Goutieres syndrome 41 test
Aicardi-Goutieres syndrome 51 test
Aicardi-Goutieres syndrome 61 test
Aicardi-Goutieres syndrome 71 test
Alagille syndrome due to a JAG1 point mutation2 tests
Alagille syndrome due to a NOTCH2 point mutation4 tests
Alpha-1-antitrypsin deficiency1 test
Alstrom syndrome1 test
Alveolar capillary dysplasia with pulmonary venous misalignment3 tests
Aneurysm-osteoarthritis syndrome1 test
Angelman syndrome2 tests
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis2 tests
Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis2 tests
Aortic aneurysm, familial thoracic 101 test
Aortic aneurysm, familial thoracic 11, susceptibility to1 test
Aortic aneurysm, familial thoracic 41 test
Aortic aneurysm, familial thoracic 61 test
Aortic aneurysm, familial thoracic 71 test
Aortic aneurysm, familial thoracic 81 test
Aortic aneurysm, familial thoracic 91 test
Aortic valve disease 21 test
Arginine:glycine amidinotransferase deficiency1 test
Arterial tortuosity syndrome1 test
Arthrogryposis, renal dysfunction, and cholestasis 11 test
Arthrogryposis, renal dysfunction, and cholestasis 21 test
Ataxia - oculomotor apraxia type 41 test
Ataxia-telangiectasia syndrome1 test
Atrial fibrillation, familial, 72 tests
Atypical hemolytic-uremic syndrome2 tests
Atypical hemolytic-uremic syndrome with C3 anomaly1 test
Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly2 tests
Atypical hemolytic-uremic syndrome with thrombomodulin anomaly1 test
Auriculocondylar syndrome 11 test
Auriculocondylar syndrome 21 test
Auriculocondylar syndrome 31 test
Autism spectrum disorder1 test
Autoimmune interstitial lung disease-arthritis syndrome3 tests
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency1 test
Autoimmune lymphoproliferative syndrome type 41 test
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD1 test
Autoinflammatory syndrome, familial, Behcet-like2 tests
Autosomal dominant nocturnal frontal lobe epilepsy 51 test
Autosomal dominant nonsyndromic hearing loss 131 test
Autosomal dominant osteopetrosis 21 test
Autosomal recessive nonsyndromic hearing loss 1A1 test
Autosomal recessive osteopetrosis 11 test
Autosomal recessive osteopetrosis 21 test
Autosomal recessive osteopetrosis 51 test
Autosomal recessive osteopetrosis 61 test
Autosomal recessive osteopetrosis 81 test
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 191 test
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 201 test
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 41 test
Baller-Gerold syndrome2 tests
Bardet-Biedl syndrome 11 test
Bardet-Biedl syndrome 101 test
Bardet-Biedl syndrome 121 test
Bardet-Biedl syndrome 131 test
Bardet-Biedl syndrome 141 test
Bardet-Biedl syndrome 151 test
Bardet-Biedl syndrome 161 test
Bardet-Biedl syndrome 21 test
Bardet-Biedl syndrome 221 test
Bardet-Biedl syndrome 41 test
Bardet-Biedl syndrome 51 test
Bardet-Biedl syndrome 71 test
Bardet-Biedl syndrome 91 test
Basal cell carcinoma, susceptibility to, 11 test
Basal laminar drusen1 test
Benign familial hematuria1 test
Benign hereditary chorea1 test
Benign recurrent intrahepatic cholestasis type 11 test
Benign recurrent intrahepatic cholestasis type 21 test
Biotinidase deficiency1 test
Bohring-Opitz syndrome1 test
Bone fragility with contractures, arterial rupture, and deafness1 test
Borjeson-Forssman-Lehmann syndrome1 test
Brachydactyly type A1D1 test
Brain-lung-thyroid syndrome1 test
Branchiootic syndrome 32 tests
Branchiootorenal syndrome 22 tests
C syndrome2 tests
C1Q deficiency1 test
CFHR5 deficiency1 test
CHARGE syndrome3 tests
Capillary malformation-arteriovenous malformation 11 test
Carcinoma of pancreas1 test
Cardiofaciocutaneous syndrome 31 test
Carotid intimal medial thickness 11 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
Cerebral arteriovenous malformation1 test
Cerebral folate transport deficiency1 test
Cerebro-costo-mandibular syndrome1 test
Cernunnos-XLF deficiency1 test
Chitayat syndrome2 tests
Cholestasis, intrahepatic, of pregnancy, 31 test
Cholestasis, progressive familial intrahepatic, 41 test
Cholestasis, progressive familial intrahepatic, 51 test
Christianson syndrome1 test
Chylomicron retention disease1 test
Ciliary dyskinesia, primary, 372 tests
Citrullinemia type II1 test
Classic homocystinuria1 test
Cleidocranial dysostosis2 tests
Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome2 tests
Cohen syndrome1 test
Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness1 test
Combined immunodeficiency due to DOCK8 deficiency1 test
Combined immunodeficiency due to LRBA deficiency1 test
Combined immunodeficiency due to partial RAG1 deficiency1 test
Combined immunodeficiency with skin granulomas1 test
Combined immunodeficiency, X-linked1 test
Complement component 3 deficiency1 test
Complement component 4a deficiency1 test
Complement component 4b deficiency1 test
Complement component 6 deficiency1 test
Complement component 7 deficiency1 test
Complement component 9 deficiency1 test
Complement component C1s deficiency1 test
Complement factor b deficiency1 test
Congenital bilateral aplasia of vas deferens from CFTR mutation3 tests
Congenital bile acid synthesis defect 11 test
Congenital bile acid synthesis defect 21 test
Congenital central hypoventilation1 test
Congenital chromosomal disease1 test
Congenital contractural arachnodactyly1 test
Congenital diarrhea 7 with exudative enteropathy1 test
Congenital generalized lipodystrophy type 31 test
Congenital glucose-galactose malabsorption1 test
Congenital heart defects, multiple types, 51 test
Congenital lactase deficiency1 test
Congenital malabsorptive diarrhea 41 test
Congenital microvillous atrophy2 tests
Congenital muscular hypertrophy-cerebral syndrome1 test
Congenital secretory diarrhea, chloride type1 test
Congenital secretory sodium diarrhea 31 test
Congenital secretory sodium diarrhea 81 test
Conotruncal heart malformations1 test
Corneal dystrophy, Fuchs endothelial, 31 test
Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome1 test
Cornelia de Lange syndrome 11 test
Cornelia de Lange syndrome 31 test
Cornelia de Lange syndrome 51 test
Cortical dysplasia-focal epilepsy syndrome1 test
Cranioectodermal dysplasia 12 tests
Cranioectodermal dysplasia 22 tests
Cranioectodermal dysplasia 32 tests
Cranioectodermal dysplasia 41 test
Craniofacial-deafness-hand syndrome1 test
Craniofrontonasal syndrome2 tests
Craniosynostosis 22 tests
Craniosynostosis 62 tests
Creatine transporter deficiency1 test
Cryptosporidiosis-chronic cholangitis-liver disease syndrome1 test
Curry-Hall syndrome1 test
Cushing syndrome1 test
Cutis laxa, autosomal recessive, type 1A1 test
Cutis laxa, autosomal recessive, type 1B1 test
Cyclical neutropenia1 test
Cystic fibrosis3 tests
DNA ligase IV deficiency1 test
DYRK1A-related intellectual disability syndrome1 test
Deafness, congenital heart defects, and posterior embryotoxon2 tests
Deafness-lymphedema-leukemia syndrome2 tests
Deficiency of 3-hydroxyacyl-CoA dehydrogenase2 tests
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
Deficiency of acetyl-CoA acetyltransferase2 tests
Deficiency of galactokinase1 test
Deficiency of guanidinoacetate methyltransferase1 test
Dermatofibrosis lenticularis disseminata1 test
Developmental and epileptic encephalopathy, 11 test
Developmental and epileptic encephalopathy, 111 test
Developmental and epileptic encephalopathy, 21 test
Developmental and epileptic encephalopathy, 261 test
Developmental and epileptic encephalopathy, 271 test
Developmental and epileptic encephalopathy, 461 test
Developmental and epileptic encephalopathy, 581 test
Developmental and epileptic encephalopathy, 71 test
Developmental and epileptic encephalopathy, 91 test
Diabetes mellitus, transient neonatal, 32 tests
Dilated cardiomyopathy 1NN1 test
Dubin-Johnson syndrome1 test
Dyskeratosis congenita, X-linked2 tests
Dyskeratosis congenita, autosomal dominant 11 test
Dystonia 91 test
Ectodermal dysplasia and immunodeficiency 12 tests
Eculizumab, poor response to1 test
Ehlers-Danlos syndrome1 test
Ehlers-Danlos syndrome, cardiac valvular type1 test
Ehlers-Danlos syndrome, classic type, 21 test
Ehlers-Danlos syndrome, kyphoscoliotic type 11 test
Ehlers-Danlos syndrome, periodontal type 11 test
Ehlers-Danlos syndrome, type 42 tests
Ellis-van Creveld syndrome1 test
Encephalocraniocutaneous lipomatosis2 tests
Epilepsy2 tests
Epiphyseal dysplasia, multiple, 61 test
Exudative vitreoretinopathy 41 test
FG syndrome 21 test
Familial Mediterranean fever2 tests
Familial cold autoinflammatory syndrome 11 test
Familial cold autoinflammatory syndrome 22 tests
Familial cold autoinflammatory syndrome 31 test
Familial expansile osteolysis1 test
Familial pulmonary capillary hemangiomatosis2 tests
Familial spontaneous pneumothorax1 test
Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young2 tests
Fanconi-Bickel syndrome1 test
Feingold syndrome type 11 test
Fibrochondrogenesis 11 test
Fibromatosis, gingival, 11 test
Fibrous dysplasia of jaw1 test
Fragile X syndrome1 test
Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome1 test
Frontonasal dysplasia with alopecia and genital anomaly1 test
Frontorhiny1 test
Fructose-biphosphatase deficiency1 test
Galactosemia1 test
Generalized epilepsy with febrile seizures plus, type 21 test
Generalized pustular psoriasis1 test
Global developmental delay1 test
Glucose-6-phosphate transport defect1 test
Glycogen storage disease IXa12 tests
Glycogen storage disease IXb2 tests
Glycogen storage disease IXc2 tests
Glycogen storage disease IXd1 test
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA2 tests
Glycogen storage disease type III2 tests
Glycogen storage disease, type II1 test
Glycogen storage disease, type IV1 test
Glycogen storage disease, type VI2 tests
Glycogen storage disease, type VII1 test
Glycogen storage disorder due to hepatic glycogen synthase deficiency2 tests
Granulomatous disease, chronic, X-linked1 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative1 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 11 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 21 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 31 test
Greig cephalopolysyndactyly syndrome1 test
H syndrome1 test
Hearing loss, autosomal dominant 34, with or without inflammation1 test
Hemolytic uremic syndrome, atypical, susceptibility to, 12 tests
Hereditary angioedema type 11 test
Hereditary disease2 tests
Hereditary pancreatitis1 test
Heterotopia, periventricular, X-linked dominant1 test
Histiocytic medullary reticulosis1 test
Hyper-IgM syndrome type 11 test
Hyper-IgM syndrome type 21 test
Hyper-IgM syndrome type 51 test
Hypercholanemia, familial 11 test
Hypercholesterolemia, autosomal dominant, type B1 test
Hyperinsulinism-hyperammonemia syndrome2 tests
Hypomyelinating leukodystrophy 111 test
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome1 test
IL21-related infantile inflammatory bowel disease1 test
Immunodeficiency 1041 test
Immunodeficiency 141 test
Immunodeficiency due to MASP-2 deficiency1 test
Immunodeficiency due to ficolin3 deficiency1 test
Immunodeficiency, common variable, 11 test
Immunodeficiency, common variable, 101 test
Immunodeficiency, common variable, 121 test
Immunodeficiency, common variable, 71 test
Immunoglobulin-mediated membranoproliferative glomerulonephritis1 test
Infantile nephronophthisis2 tests
Infantile-onset periodic fever-panniculitis-dermatosis syndrome1 test
Inflammatory bowel disease 11 test
Inflammatory skin and bowel disease, neonatal, 11 test
Insulin-resistant diabetes mellitus AND acanthosis nigricans1 test
Intellectual disability, autosomal dominant 11 test
Intellectual disability, autosomal dominant 201 test
Interstitial lung disease due to ABCA3 deficiency2 tests
Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked1 test
Ischemic stroke1 test
Joubert syndrome 101 test
Juvenile myelomonocytic leukemia1 test
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome1 test
KBG syndrome1 test
Kabuki syndrome 11 test
Kabuki syndrome 21 test
Kartagener syndrome2 tests
Kleefstra syndrome 11 test
LEOPARD syndrome 11 test
Lafora disease1 test
Landau-Kleffner syndrome1 test
Langer mesomelic dysplasia syndrome1 test
Larsen-like syndrome, B3GAT3 type1 test
Legius syndrome1 test
Lethal osteosclerotic bone dysplasia1 test
Leukocyte adhesion deficiency 31 test
Loeys-Dietz syndrome 12 tests
Loeys-Dietz syndrome 21 test
Loeys-Dietz syndrome 41 test
Lung carcinoma1 test
Luscan-Lumish syndrome1 test
Lymphoproliferative syndrome 21 test
Lynch syndrome 81 test
Lysinuric protein intolerance2 tests
Lysosomal acid lipase deficiency1 test
MEGF8-related Carpenter syndrome2 tests
Majeed syndrome2 tests
Malignant tumor of esophagus1 test
Malignant tumor of urinary bladder1 test
Mandibulofacial dysostosis-microcephaly syndrome1 test
Maple syrup urine disease1 test
Marfan syndrome2 tests
Marshall syndrome1 test
Maturity-onset diabetes of the young type 11 test
Maturity-onset diabetes of the young type 111 test
Maturity-onset diabetes of the young type 141 test
Maturity-onset diabetes of the young type 41 test
Maturity-onset diabetes of the young type 61 test
Maturity-onset diabetes of the young type 71 test
Maturity-onset diabetes of the young type 81 test
Meconium ileus1 test
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency1 test
Metabolic myopathy due to lactate transporter defect3 tests
Mevalonic aciduria2 tests
Microvascular complications of diabetes, susceptibility to, 41 test
Miller syndrome1 test
Monocytopenia with susceptibility to infections1 test
Mowat-Wilson syndrome1 test
Multiple congenital anomalies1 test
Multiple sclerosis, susceptibility to, 52 tests
Mungan syndrome1 test
Myhre syndrome1 test
Myoclonus, familial, 21 test
Nager syndrome1 test
Neonatal ichthyosis-sclerosing cholangitis syndrome1 test
Neonatal severe primary hyperparathyroidism1 test
Niemann-Pick disease, type C11 test
Niemann-Pick disease, type C21 test
Noonan syndrome1 test
Noonan syndrome 101 test
Noonan syndrome 111 test
Noonan syndrome 81 test
Noonan syndrome 91 test
Noonan syndrome-like disorder with loose anagen hair 11 test
Noonan syndrome-like disorder with loose anagen hair 21 test
OBESITY (BMIQ9), SUSCEPTIBILITY TO1 test
Obesity1 test
Obesity due to congenital leptin deficiency1 test
Obesity due to leptin receptor gene deficiency1 test
Obesity due to pro-opiomelanocortin deficiency1 test
Obesity due to prohormone convertase I deficiency2 tests
Oculomaxillofacial dysostosis2 tests
Osteogenesis imperfecta1 test
Osteogenesis imperfecta type I1 test
Osteogenesis imperfecta with normal sclerae, dominant form1 test
Osteopathia striata with cranial sclerosis1 test
Osteopetrosis with renal tubular acidosis1 test
Otitis media, susceptibility to1 test
Oto-palato-digital syndrome, type I1 test
Otofaciocervical syndrome 12 tests
PGM1-congenital disorder of glycosylation1 test
PMM2-congenital disorder of glycosylation1 test
Pancreatic triacylglycerol lipase deficiency1 test
Pancytopenia due to IKZF1 mutations1 test
Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome1 test
Periodic fever-infantile enterocolitis-autoinflammatory syndrome1 test
Phenylketonuria1 test
Phosphate transport defect1 test
Phosphoenolpyruvate carboxykinase deficiency, cytosolic1 test
Pitt-Hopkins-like syndrome 21 test
Primary CD59 deficiency1 test
Primary ciliary dyskinesia2 tests
Primary ciliary dyskinesia 102 tests
Primary ciliary dyskinesia 112 tests
Primary ciliary dyskinesia 122 tests
Primary ciliary dyskinesia 132 tests
Primary ciliary dyskinesia 142 tests
Primary ciliary dyskinesia 152 tests
Primary ciliary dyskinesia 162 tests
Primary ciliary dyskinesia 172 tests
Primary ciliary dyskinesia 182 tests
Primary ciliary dyskinesia 192 tests
Primary ciliary dyskinesia 22 tests
Primary ciliary dyskinesia 202 tests
Primary ciliary dyskinesia 212 tests
Primary ciliary dyskinesia 222 tests
Primary ciliary dyskinesia 232 tests
Primary ciliary dyskinesia 242 tests
Primary ciliary dyskinesia 252 tests
Primary ciliary dyskinesia 262 tests
Primary ciliary dyskinesia 272 tests
Primary ciliary dyskinesia 282 tests
Primary ciliary dyskinesia 292 tests
Primary ciliary dyskinesia 32 tests
Primary ciliary dyskinesia 302 tests
Primary ciliary dyskinesia 322 tests
Primary ciliary dyskinesia 332 tests
Primary ciliary dyskinesia 52 tests
Primary ciliary dyskinesia 62 tests
Primary ciliary dyskinesia 72 tests
Primary ciliary dyskinesia 92 tests
Progeroid and marfanoid aspect-lipodystrophy syndrome1 test
Progressive sclerosing poliodystrophy1 test
Properdin deficiency, X-linked1 test
Proteasome-associated autoinflammatory syndrome 12 tests
Pseudo-TORCH syndrome 21 test
Psoriasis 15, pustular, susceptibility to1 test
Psoriasis 21 test
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 21 test
Pulmonary hypertension, primary, 12 tests
Pulmonary hypertension, primary, 22 tests
Pulmonary hypertension, primary, 42 tests
Purine-nucleoside phosphorylase deficiency1 test
Pyknodysostosis1 test
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome2 tests
Pyridoxal phosphate-responsive seizures1 test
Pyridoxine-dependent epilepsy1 test
RAB23-related Carpenter syndrome2 tests
Recurrent Neisseria infections due to factor D deficiency1 test
Retinitis pigmentosa 231 test
Retinitis pigmentosa 31 test
Retinitis pigmentosa 511 test
Retinitis pigmentosa 551 test
Retinitis pigmentosa 711 test
Retinitis pigmentosa and erythrocytic microcytosis1 test
Rett syndrome, congenital variant1 test
Rienhoff syndrome1 test
Rubinstein-Taybi syndrome due to CREBBP mutations1 test
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency1 test
STAT3-related early-onset multisystem autoimmune disease1 test
STING-associated vasculopathy with onset in infancy1 test
Sarcotubular myopathy1 test
Schaaf-Yang syndrome1 test
Schuurs-Hoeijmakers syndrome1 test
Severe combined immunodeficiency disease1 test
Severe combined immunodeficiency due to DNA-PKcs deficiency1 test
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency1 test
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency2 tests
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome1 test
Severe neonatal-onset encephalopathy with microcephaly1 test
Sex chromosome disorder of sex development1 test
Short stature-brachydactyly-obesity-global developmental delay syndrome1 test
Shprintzen-Goldberg syndrome3 tests
Spastic paraplegia, intellectual disability, nystagmus, and obesity1 test
Spinal muscular atrophy1 test
Spondyloenchondrodysplasia with immune dysregulation1 test
Stickler syndrome1 test
Sucrase-isomaltase deficiency1 test
Supravalvar aortic stenosis1 test
Surfactant metabolism dysfunction, pulmonary, 12 tests
Surfactant metabolism dysfunction, pulmonary, 22 tests
Surfactant metabolism dysfunction, pulmonary, 42 tests
Surfactant metabolism dysfunction, pulmonary, 52 tests
Systemic lupus erythematosus2 tests
T-B+ severe combined immunodeficiency due to JAK3 deficiency1 test
T-cell immunodeficiency, congenital alopecia, and nail dystrophy1 test
TCF12-related craniosynostosis2 tests
TWIST1-related craniosynostosis2 tests
Telangiectasia, hereditary hemorrhagic, type 12 tests
Telangiectasia, hereditary hemorrhagic, type 22 tests
Telangiectasia, hereditary hemorrhagic, type 52 tests
Thrombomodulin-related bleeding disorder1 test
Townes-Brocks syndrome 11 test
Treacher Collins syndrome 11 test
Treacher Collins syndrome 21 test
Trichohepatoenteric syndrome 11 test
Trichohepatoenteric syndrome 21 test
Type 1 diabetes mellitus 21 test
Type 1 diabetes mellitus 203 tests
Type 2 diabetes mellitus3 tests
Type I complement component 8 deficiency1 test
Type II complement component 8 deficiency1 test
UDPglucose-4-epimerase deficiency1 test
Unverricht-Lundborg syndrome1 test
Vasculitis due to ADA2 deficiency3 tests
Waardenburg syndrome type 11 test
Waardenburg syndrome type 2D1 test
Waardenburg syndrome type 4C1 test
Warts, hypogammaglobulinemia, infections, and myelokathexis1 test
X-linked Alport syndrome2 tests
X-linked agammaglobulinemia1 test
X-linked cone-rod dystrophy 11 test
X-linked intellectual disability Cabezas type1 test
X-linked intellectual disability with marfanoid habitus1 test
X-linked intellectual disability-cerebellar hypoplasia syndrome1 test
X-linked lymphoproliferative disease due to SH2D1A deficiency1 test
X-linked lymphoproliferative disease due to XIAP deficiency1 test
X-linked reticulate pigmentary disorder1 test
X-linked severe congenital neutropenia1 test