All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00511 614924 Combined oxidative phosphorylation deficiency 12, 614924 (3) 614924 0 0 EARS2 - -