Disease #00105

Official abbreviation	605911
Name	HMG-CoA synthase-2 deficiency, 605911 (3);MITOCHONDRIAL HMG-CoA SYNTHASE DEFICIENCY
OMIM ID	605911
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	HMGCS2
Associated tissues	-
Disease features	-
Remarks	-