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Diseases
Genes (1031)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
TSLP
Cholera
Membranoproliferative Glomerulonephritis
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
SHH
Cyclopia
SLC4A4
Proximal Renal Tubular Acidosis
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
FUT2
Norovirus Infection
SOST
Craniodiaphyseal Dysplasia
LEMD3
Melorheostosis
ALB
Cholera
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Disinhibition