Disease #03834 (CEMCOX2 (cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency, type 2 (CEMCOX-2)), OMIM:615119)

Official abbreviation CEMCOX2
Name cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency, type 2 (CEMCOX-2)
OMIM ID 615119
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene COX15
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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