All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00096 COXPD2 Combined oxidative phosphorylation deficiency 2, 610498 (3) 610498 0 0 MRPS16 - -