Disease #00106

Official abbreviation 238970
Name Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3)
OMIM ID 238970
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SLC25A15
Associated tissues -
Disease features -
Remarks -

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