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Diseases
Genes (1325)
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RB1
Pinealoblastoma
Trilateral Retinoblastoma
Retinoblastoma
ASL
Argininosuccinic Aciduria
ARID1B
Coffin-Siris Syndrome 2
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
ATR
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
Coffin-Siris Syndrome 2
Retinoblastoma
FLVCR1
Posterior Column Ataxia With Retinitis Pigmentosa
PQBP1
Renpenning's Syndrome
CENPJ
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ARID1A
Coffin-Siris Syndrome 2
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
SMARCE1
Coffin-Siris Syndrome 2
SOX11
Coffin-Siris Syndrome 2
ACTG2
Berdon Syndrome
SMARCA4
Coffin-Siris Syndrome 2
Vascular Tumor
Retinoblastoma
PCNT
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
DMPK
Myotonic Dystrophy