All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00529 616277 Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3) 616277 0 0 ECHS1 - -