CORIN, corin, serine peptidase, 10699

N. diseases: 55; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly
0.210 GeneticVariation phenotype LHGDN Corin variant associated with hypertension and cardiac hypertrophy exhibits impaired zymogen activation and natriuretic peptide processing activity. 18669922 2008
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly
0.210 Biomarker phenotype RGD Upregulation of corin gene expression in hypertrophic cardiomyocytes and failing myocardium. 15191894 2004