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Diseases
Genes (1087)
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ABHD5
Cerebral Creatine Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Hepatitis E
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis
Type Iii Hypersensitivity
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
Disinhibition
IFNG
Hepatitis E
Cerebral Creatine Deficiency
Cystinosis
Type Iii Hypersensitivity
Cryptococcosis
Congenital Contractural Arachnodactyly
Vascular Tumor
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
PRKAR1A
Alopecia, Androgenetic, 1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Vascular Tumor