ERBB3, erb-b2 receptor tyrosine kinase 3, 2065

N. diseases: 318; N. variants: 16
Disease: ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4746575
Disease: ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO
ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO 		0.400 GeneticVariation phenotype UNIPROT A germline ERBB3 variant is a candidate for predisposition to erythroid MDS/erythroleukemia. 27416908 2016
CUI: C4746575
Disease: ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO
ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO 		0.400 GeneticVariation phenotype CLINVAR