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Diseases
Genes (1092)
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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
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
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
IFNG
Cerebral Creatine Deficiency
Cryptococcosis
Cystinosis
Type Iii Hypersensitivity
Congenital Contractural Arachnodactyly
PRKAR1A
Alopecia, Androgenetic, 1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
DIAPH3
Auditory Neuropathy