All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00493 COXPD7 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7 613559 0 0 C12orf65 - -