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	-