LNPEP, leucyl and cystinyl aminopeptidase, 4012

N. diseases: 174; N. variants: 13
Disease: Beta thalassemia intermedia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		0.010 GeneticVariation disease BEFREE Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia. 26418075 2016