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Diseases
Genes (3118)
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RB1
Osteogenic Sarcoma
Retinoblastoma
Pinealoblastoma
Trilateral Retinoblastoma
TP53
Osteogenic Sarcoma
Myotonic Dystrophy
Retinoblastoma
Spinocerebellar Ataxia Type 7
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ASL
Argininosuccinic Aciduria
FOXP3
Osteogenic Sarcoma
Ipex Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
EFHC1
Myoclonic Epilepsy, Juvenile, Susceptibility To, 3
PMM2
Pmm2 Deficiency
ATXN7
Spinocerebellar Ataxia Type 7
Autosomal Dominant Cerebellar Ataxia
CHEK2
Osteogenic Sarcoma
Retinoblastoma
LMNA
Osteogenic Sarcoma
Retinoblastoma
Limb–girdle Muscular Dystrophy
AKT1
Osteogenic Sarcoma
Retinoblastoma
Amphetamine Dependence
VEGFA
Osteogenic Sarcoma
Retinoblastoma
Multiple Epiphyseal Dysplasia
PQBP1
Osteogenic Sarcoma
Renpenning's Syndrome
SLC2A10
Arterial Tortuosity Syndrome
PRPS1
Arts Syndrome
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
FAM126A
Hypomyelination And Congenital Cataract
GSTP1
Osteogenic Sarcoma
Amphetamine Dependence