All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00023 604273 Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, 604273 (3) 604273 0 0 ATPAF2 - -