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Diseases
Genes (1160)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
NIPBL
Cornelia De Lange Syndrome 3
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
RAD21
Cornelia De Lange Syndrome 3
GALE
Galactose Epimerase Deficiency
SMC1A
Cornelia De Lange Syndrome 3
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
HDAC8
Fibrous Dysplasia Of Bone
Cornelia De Lange Syndrome 3
CFH
Membranoproliferative Glomerulonephritis
FLNA
Intestinal Neuronal Dysplasia
Fg 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