Disease #04419

Official abbreviation CEMCOX-3
Name cardioencephalomyopathy?, fatal infantile, due to cytochrome C oxidase deficiency, type 3 (CEMCOX-3)
OMIM ID 616500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COA5
Associated tissues -
Disease features -
Remarks -