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DO Term : COX deficiency, benign infantile mitochondrial myopathy [DOID:0081377] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.

synonyms:
Isolated cytochrome C oxidase deficiency,
ORDO:254905,
GARD:48,
UMLS_CUI:C5779825

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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