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Diseases
Genes (3250)
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RB1
Pinealoblastoma
Osteosarcoma
Holoprosencephaly
Trilateral Retinoblastoma
Retinoblastoma
TP53
Gastrinoma
Adenoid Cystic Carcinoma
Osteosarcoma
Fibrolamellar Hepatocellular Carcinoma
Retinoblastoma
BCOR
Adenoid Cystic Carcinoma
Osteosarcoma
Retinoblastoma
TTPA
Familial Isolated Vitamin E Deficiency
PYGM
Gastrinoma
Glycogen Storage Disease Type V
MMUT
Osteosarcoma
Methylmalonyl-Coa Mutase Deficiency
Retinoblastoma
SLC2A1
Adenoid Cystic Carcinoma
Glut1 Deficiency
Osteosarcoma
Dravet Syndrome
SCN1A
Hippocampal Sclerosis
Dravet Syndrome
CHEK2
Osteosarcoma
Retinoblastoma
GNAQ
Sturge–weber Syndrome
Mongolian Spot
GLI2
Osteosarcoma
Holoprosencephaly
MED12
Fg Syndrome
SLC17A5
Salla Disease
PMM2
Cutis Laxa
Pmm2 Deficiency
PTEN
Adenoid Cystic Carcinoma
Osteosarcoma
Protein Losing Enteropathy
Thrombophlebitis
Systemic Inflammatory Response Syndrome
Retinoblastoma
SIX3
Osteosarcoma
Holoprosencephaly
ELN
Cutis Laxa
Retinoblastoma
SHH
Holoprosencephaly
TGIF1
Holoprosencephaly
FBLN5
Cutis Laxa