Disease: Familial Retinoblastoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma 		0.300 GeneticVariation disease ORPHANET Role of MYCN in retinoblastoma. 23498720 2013
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma 		0.300 GeneticVariation disease ORPHANET Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies. 23498719 2013