Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1355
Gene Symbol: COX15
COX15
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
0.500 GermlineCausalMutation ORPHANET Infantile cardioencephalopathy due to a COX15 gene defect: report and review. 21412973

2011

Entrez Id: 1355
Gene Symbol: COX15
COX15
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
0.500 GermlineCausalMutation ORPHANET Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency. 2175025

1990

Entrez Id: 1355
Gene Symbol: COX15
COX15
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
0.500 Biomarker CTD_human