All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00513 615440 Combined oxidative phosphorylation deficiency 17, 615440 (3) 615440 0 0 ELAC2 - -