Disease #03834 (CEMCOX-2 (cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency, type 2 (CEMCOX-2)), OMIM:615119)

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