All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00100 COXPD9 Combined oxidative phosphorylation deficiency 9, 614582 (3) 614582 0 0 MRPL3 - -