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Diseases
Genes (327)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
LBR
Hydrops-Ectopic Calcification-Moth-Eaten Skeletal Dysplasia
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
UMOD
Medullary Cystic Kidney Disease
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
MRAP
Familial Glucocorticoid Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma
TFE3
Epithelioid Hemangioendothelioma
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
YAP1
Epithelioid Hemangioendothelioma
TNFRSF10A
Alopecia, Androgenetic, 1
Lumbar Disc Disease
CILP
Lumbar Disc Disease