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DO Term : primary coenzyme Q10 deficiency 8 [DOID:0070245] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3.
  • synonyms:
  • OMIM:616733,
  • COQ10D8,
  • 616733,
  • coenzyme Q10 deficiency, primary, 8
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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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