All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00504 616811 ?Combined oxidative phosphorylation deficiency 29, 616811 (3) 616811 0 0 TXN2 - -