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DO Term : nuclear type mitochondrial complex I deficiency [DOID:0112065] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome.

synonyms:
OMIM:PS252010,
PS252010,
MC1DN

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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