All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00520 616794 Combined oxidative phosphorylation deficiency 28, 616794 (3) 616794 0 0 SLC25A26 - -