Disease: Thrombosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040053
Disease: Thrombosis
Thrombosis 		0.020 GeneticVariation phenotype LHGDN MPL mutations lacked prognostic significance with respect to thrombosis, major hemorrhage, myelofibrotic transformation or survival. 18451306 2008
CUI: C0040053
Disease: Thrombosis
Thrombosis 		0.020 AlteredExpression phenotype LHGDN Thrombotic and bleeding complications in four subpopulations of patients with essential thrombocythemia defined by c-Mpl protein expression and PRV-1 mRNA levels. 15951300 2005