All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00099 COXPD5 Combined oxidative phosphorylation deficiency 5, 611719 (3) 611719 0 0 MRPS22 - -