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Summary Literature (0)
MIM:238970 - HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME; HHHS

Xenbase Genes: slc25a15.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009393 - ornithine translocase deficiency

Disease Ontology (DO):
DOID:0050720 - ornithine translocase deficiency