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DO Term : mitochondrial complex III deficiency nuclear type 3 [DOID:0080112] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRB gene on chromosome 8q22.

synonyms:
615158,
OMIM:615158

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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