All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00516 616198 Combined oxidative phosphorylation deficiency 23, 616198 (3) 616198 0 0 GTPBP3 - -