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Diseases
Genes (1431)
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ASL
Argininosuccinic Aciduria
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
TNFAIP3
Haploinsufficiency Of A20
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
GALE
Galactose Epimerase Deficiency
AVP
Diabetes Insipidus
IFIH1
Singleton Merten Syndrome
FGFR2
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
EGFR
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
Enamel-Renal Syndrome
CFH
Membranoproliferative Glomerulonephritis
MYH11
Aneurysm
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome
ASS1
Argininosuccinic Aciduria
Congenital Contractural Arachnodactyly
Citrullinemia Type I