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Diseases
Genes (1014)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup 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
CFH
Membranoproliferative Glomerulonephritis
Pleural Effusion
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
C1QA
Membranoproliferative Glomerulonephritis
Pleural Effusion
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma