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Diseases
Genes (1572)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
LMNA
Limb–girdle Muscular Dystrophy
Adenoid Cystic Carcinoma
Retinoblastoma
UBE3B
Kaufman Oculocerebrofacial Syndrome
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
Retinoblastoma
BCOR
Adenoid Cystic Carcinoma
Retinoblastoma
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
Retinoblastoma
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy
DES
Limb–girdle Muscular Dystrophy
CAV3
Limb–girdle Muscular Dystrophy
ASS1
Citrullinemia Type I
Retinoblastoma
VEGFA
Corneal Neovascularization
Adenoid Cystic Carcinoma
Retinoblastoma
Lymphangiosarcoma