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DO Term : mitochondrial complex V (ATP synthase) deficiency [DOID:0111143] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex.

synonyms:
UMLS_CUI:C4757950,
GARD:1459,
ORDO:254913,
SNOMEDCT_US_2023_03_01:780820008

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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