All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00080 COXPD16 Combined oxidative phosphorylation deficiency 16, 615395 (3) 615395 0 0 MRPL44 - -