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Diseases
Genes (1161)
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ASL
Argininosuccinic Aciduria
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
ALB
Cholera
Membranoproliferative Glomerulonephritis
Uveitis
Congenital Contractural Arachnodactyly
Disinhibition
CFH
Membranoproliferative Glomerulonephritis
Uveitis
IL1B
Cholera
Membranoproliferative Glomerulonephritis
Cystinosis
Uveitis
Congenital Contractural Arachnodactyly
Renpenning's Syndrome
TSLP
Cholera
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
CCL2
Membranoproliferative Glomerulonephritis
Cystinosis
Uveitis
IL6
Argininosuccinic Aciduria
Cholera
Membranoproliferative Glomerulonephritis
Uveitis
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Dysentery
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Cholera
Uveitis
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Dysentery
PRKACA
Fibrolamellar Hepatocellular Carcinoma