Disease: Splenomegaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038002
Disease: Splenomegaly
Splenomegaly 		0.300 Biomarker phenotype CTD_human STAT5BN642H is a driver mutation for T cell neoplasia. 29200404 2018