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DO Term : nuclear type mitochondrial complex I deficiency 30 [DOID:0112098] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFB11 gene on chromosome Xp11.3.

synonyms:
301021,
MC1DN30,
OMIM:301021

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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