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Diseases
Genes (1159)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
CFH
Membranoproliferative Glomerulonephritis
MYH11
Aneurysm
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome
TP53
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Adenoid Cystic Carcinoma
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
PTEN
Membranoproliferative Glomerulonephritis
Thrombophlebitis
Protein Losing Enteropathy
Congenital Contractural Arachnodactyly
Adenoid Cystic Carcinoma
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
PIK3CA
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Adenoid Cystic Carcinoma
CTNS
Cystinosis