Disease #00482

Official abbreviation	CEMCOX1
Name	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1
OMIM ID	604377
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	SCO2
Associated tissues	-
Disease features	-
Remarks	-