All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00411 COXPD6 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6 300816 0 0 AIFM1 - -