Disease #00641

Official abbreviation	615119
Name	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2
OMIM ID	615119
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	COX15
Associated tissues	-
Disease features	-
Remarks	-