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Diseases
Genes (1180)
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ATRX
Alpha-Thalassemia Mental Retardation Syndrome
Adenoid Cystic Carcinoma
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Alpha-Thalassemia Mental Retardation Syndrome
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
TP53
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Alpha-Thalassemia Mental Retardation Syndrome
Adenoid Cystic Carcinoma
CFH
Membranoproliferative Glomerulonephritis
MYH11
Aneurysm
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome
PTEN
Membranoproliferative Glomerulonephritis
Thrombophlebitis
Protein Losing Enteropathy
Congenital Contractural Arachnodactyly
Alpha-Thalassemia Mental Retardation Syndrome
Adenoid Cystic Carcinoma
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
PIK3CA
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Adenoid Cystic Carcinoma