All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00641 615119 Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 615119 0 0 COX15 - -