All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00106 238970 Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3) 238970 0 0 SLC25A15 - -