All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00523 617664 Combined oxidative phosphorylation deficiency 32, 617664 (3) 617664 0 0 MRPS34 - -