Disease: Blood Platelet Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders 		0.300 Biomarker group GENOMICS_ENGLAND A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies. 26936507 2016