All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00517 616239 Combined oxidative phosphorylation deficiency 24, 616239 (3) 616239 0 0 NARS2 - -