All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00524 617713 Combined oxidative phosphorylation deficiency 33, 617713 (3) 617713 0 0 C1QBP - -