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Diseases
Genes (2684)
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RB1
Pinealoblastoma
Holoprosencephaly
Trilateral Retinoblastoma
Osteosarcoma
TTPA
Familial Isolated Vitamin E Deficiency
TP53
Fibrolamellar Hepatocellular Carcinoma
Osteosarcoma
MMUT
Osteosarcoma
Methylmalonyl-Coa Mutase Deficiency
SLC2A1
Glut1 Deficiency
Osteosarcoma
PQBP1
Renpenning's Syndrome
Osteosarcoma
GLI2
Holoprosencephaly
Osteosarcoma
GNAQ
Sturge–weber Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
CHEK2
Osteosarcoma
SIX3
Holoprosencephaly
Osteosarcoma
SHH
Holoprosencephaly
TGIF1
Holoprosencephaly
IFIH1
Singleton Merten Syndrome
ACTG2
Osteosarcoma
Berdon Syndrome
NODAL
Holoprosencephaly
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
RASA1
Osteosarcoma
Sturge–weber Syndrome