All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00623 MEGDEL 3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome (MEGDEL) 614739 16 16 SERAC1 - -