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DO Term : nuclear type mitochondrial complex I deficiency 8 [DOID:0112081] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS3 gene on chromosome 11p11.2.

synonyms:
618230,
MC1DN8,
OMIM:618230

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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