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DO Term : combined oxidative phosphorylation deficiency 15 [DOID:0111491] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation] in the MTFMT gene on chromosome 15q22.31.

synonyms:
OMIM:614947,
614947,
COXPD15,
ORDO:319524

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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