OCLN, occludin, 100506658

N. diseases: 195; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
0.400 Biomarker phenotype CTD_human The thiopurine methyltransferase genetic polymorphism is associated with thioguanine-related veno-occlusive disease of the liver in children with acute lymphoblastic leukemia. 17015055 2006
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
0.400 Biomarker phenotype HPO