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Diseases
Genes (1550)
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UNC119
Immunodeficiency 13
Unc119 Lipid-Binding Chaperone
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
TNFAIP3
Haploinsufficiency Of A20
FH
Hereditary Leiomyomatosis And Renal Cell Cancer
PQBP1
Renpenning's Syndrome
GALE
Galactose Epimerase Deficiency
GAD1
Cerebral Palsy, Spastic Quadriplegic, 1
IFIH1
Singleton Merten Syndrome
Rotaviral Gastroenteritis
FGFR2
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
EGFR
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
CFH
Membranoproliferative Glomerulonephritis
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
DDR2
Squamous-Cell Carcinoma Of The Lung
KRAS
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
AIPL1
Unc119 Lipid-Binding Chaperone
FGFR1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung