All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00423 COXPD11 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11 614922 0 0 RMND1 - -