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Diseases
Genes (413)
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ABHD5
Cerebral Creatine Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
MYO5B
Microvillus Inclusion Disease
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma
TFE3
Epithelioid Hemangioendothelioma
TWIST1
Sweeney-Cox Syndrome
MRAP
Familial Glucocorticoid Deficiency
YAP1
Epithelioid Hemangioendothelioma
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
LEMD3
Melorheostosis
TNFRSF10A
Alopecia, Androgenetic, 1
Lumbar Disc Disease
CILP
Lumbar Disc Disease
ABCC2
Alopecia, Androgenetic, 1
SUPV3L1
Alopecia, Androgenetic, 1