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Diseases
Genes (1071)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
BRAF
Congenital Contractural Arachnodactyly
Langerhans Cell Histiocytosis
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
CD55
Cholera
Protein Losing Enteropathy
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Cholera
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
SOST
Craniodiaphyseal Dysplasia
Langerhans Cell Histiocytosis
FUT2
Norovirus Infection
ALB
Cholera
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
Congenital Contractural Arachnodactyly
Disinhibition
DDX58
Singleton Merten Syndrome