All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00512 614932 Combined oxidative phosphorylation deficiency 13, 614932 (3) 614932 0 0 PNPT1 - -