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Diseases
Genes (977)
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FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Disinhibition
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
PDGFB
Callosity
Primary Familial Brain Calcification
Liver Injury
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
FBN1
Congenital Contractural Arachnodactyly
Proximal Renal Tubular Acidosis
Liver Injury
FN1
Membranoproliferative Glomerulonephritis
Liver Injury
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
IL6
Callosity
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Liver Injury
Familial Isolated Vitamin E Deficiency
SOST
Callosity
Craniodiaphyseal Dysplasia