All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00501 615918 ?Combined oxidative phosphorylation deficiency 21, 615918 (3) 615918 0 0 TARS2 - -