All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00519 616672 Combined oxidative phosphorylation deficiency 27, 616672 (3) 616672 0 0 CARS2 - -