All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00515 615917 Combined oxidative phosphorylation deficiency 20, 615917 (3) 615917 0 0 VARS2 - -