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Diseases
Genes (3041)
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RB1
Retinoblastoma
Osteogenic Sarcoma
Pinealoblastoma
Trilateral Retinoblastoma
TP53
Retinoblastoma
Osteogenic Sarcoma
Myotonic Dystrophy
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ASL
Argininosuccinic Aciduria
VEGFA
Retinoblastoma
Osteogenic Sarcoma
Multiple Epiphyseal Dysplasia
Experimental Autoimmune Encephalomyelitis
Lymphangiosarcoma
FOXP3
Osteogenic Sarcoma
Ipex Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
CHEK2
Retinoblastoma
Osteogenic Sarcoma
SLC2A10
Arterial Tortuosity Syndrome
Aneurysm
FLNA
Multiple Epiphyseal Dysplasia
Intestinal Neuronal Dysplasia
Fg Syndrome
LMNA
Retinoblastoma
Osteogenic Sarcoma
Limb–girdle Muscular Dystrophy
PQBP1
Osteogenic Sarcoma
Renpenning's Syndrome
CAV3
Limb–girdle Muscular Dystrophy
Experimental Autoimmune Encephalomyelitis
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
PRPS1
Arts Syndrome
SIRT1
Retinoblastoma
Osteogenic Sarcoma
Renpenning's Syndrome
Experimental Autoimmune Encephalomyelitis
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency