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DO Term : mitochondrial complex V (ATP synthase) deficiency nuclear type 7 [DOID:0070464] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the ATP5PO gene on chromosome 21q22.11.
  • synonyms:
  • MC5DN7,
  • 620359,
  • OMIM:620359
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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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