Disease #00643

Official abbreviation	616501
Name	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
OMIM ID	616501
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	COA6
Associated tissues	-
Disease features	-
Remarks	-