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Diseases
Genes (458)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GNAS
Mccune-Albright Syndrome
GALE
Galactose Epimerase Deficiency
MC2R
Familial Glucocorticoid Deficiency
CFH
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
CTNS
Cystinosis
SRD5A2
Alopecia, Androgenetic, 1
AR
Placental Site Trophoblastic Tumor
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
SOST
Craniodiaphyseal Dysplasia
PRKAR1A
Alopecia, Androgenetic, 1
Mccune-Albright Syndrome
Fibrolamellar Hepatocellular Carcinoma