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Disease association ontology term - MONDO:0014668 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

Term summary

ID
MONDO:0014668
Name
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4
Ontology or CV name
Disease association
Definition
Any fatal infantile encephalocardiomyopathy in which the cause of the disease is a mutation in the COA6 gene.

Parents

Annotation

Disease association

MONDO:0014668 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

References:

Genes: