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Diseases
Genes (1203)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
F8
Haemophilia A
ATP7B
Wilson's Disease
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
EDN1
Membranoproliferative Glomerulonephritis
Erectile Dysfunction
IFIH1
Singleton Merten Syndrome
IL6
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Haemophilia A
Dysentery
Erectile Dysfunction
Wilson's Disease
TNF
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Haemophilia A
Dysentery
Erectile Dysfunction
Wilson's Disease
PDGFB
Primary Familial Brain Calcification
Erectile Dysfunction
CFH
Membranoproliferative Glomerulonephritis
NOS3
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Erectile Dysfunction
BCL2
Congenital Contractural Arachnodactyly
Erectile Dysfunction
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis