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DO Term : mitochondrial complex IV deficiency nuclear type 15 [DOID:0070500] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX8A gene on chromosome 11q13.1.

synonyms:
619059,
MC4DN15,
OMIM:619059,
UMLS_CUI:C5436712

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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