MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Neonatal Alloimmune Thrombocytopenia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		0.010 GeneticVariation disease BEFREE MYH9-macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopenia. 29286575 2018