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Diseases
Genes (1345)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
F12
Factor Xii Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
Retinoblastoma