Disease table of CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2 OMIM ID: 615119

Gene-disease associations table

GeneAssociated with CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2 inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
COX15ClinVar, OMIM, HUMSAVARHGNC link10q24.23256000, PS601462, 615119

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