All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00514 615578 Combined oxidative phosphorylation deficiency 18, 615578 (3) 615578 0 0 SFXN4 - -