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Diseases
Genes (3309)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Osteogenic Sarcoma
Retinoblastoma
TP53
Prostatic Hyperplasia, Benign
Osteogenic Sarcoma
Retinoblastoma
Adenoid Cystic Carcinoma
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
FOXP3
Prostatic Hyperplasia, Benign
Osteogenic Sarcoma
Ipex Syndrome
BCOR
Osteogenic Sarcoma
Retinoblastoma
Adenoid Cystic Carcinoma
TTPA
Familial Isolated Vitamin E Deficiency
VEGFA
Prostatic Hyperplasia, Benign
Osteogenic Sarcoma
Retinoblastoma
Multiple Epiphyseal Dysplasia
Adenoid Cystic Carcinoma
Lymphangiosarcoma
SLC2A10
Arterial Tortuosity Syndrome
Aneurysm
FLNA
Multiple Epiphyseal Dysplasia
Intestinal Neuronal Dysplasia
Fg Syndrome
CHEK2
Osteogenic Sarcoma
Retinoblastoma
PQBP1
Osteogenic Sarcoma
Renpenning's Syndrome
PTEN
Prostatic Hyperplasia, Benign
Thrombophlebitis
Protein Losing Enteropathy
Osteogenic Sarcoma
Retinoblastoma
Adenoid Cystic Carcinoma
MED12
Fg Syndrome
PRPS1
Arts Syndrome
FAM20A
Enamel-Renal Syndrome
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
COL9A1
Osteogenic Sarcoma
Multiple Epiphyseal Dysplasia
IFIH1
Singleton Merten Syndrome