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Diseases
Genes (1487)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
TTPA
Familial Isolated Vitamin E Deficiency
POLG
Balo Concentric Sclerosis
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
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
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
Retinoblastoma
CD55
Protein Losing Enteropathy