MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Immune thrombocytopenic purpura ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		0.010 GeneticVariation disease BEFREE R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura. 23759689 2014