SLC25A15 variants [mitochondrial inner membrane]

Stable Identifier
R-HSA-9956499
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
mitochondrial inner membrane
Locations in the PathwayBrowser
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Participants
members
candidates
Disease
Name Identifier Synonyms
ornithine translocase deficiency DOID:0050720 Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome, HHH syndrome
Cross References
Mondo
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