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DO Term : mitochondrial complex V (ATP synthase) deficiency nuclear type 3 [DOID:0060332] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5E gene on chromosome 20q13.

synonyms:
614053,
OMIM:614053,
MC5DN3

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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