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DO Term : primary coenzyme Q10 deficiency 4 [DOID:0070241] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the ADCK3 gene on chromosome 1q42.13.
  • synonyms:
  • 612016,
  • spinocerebellar ataxia, autosomal recessive 9,
  • GARD:10294,
  • OMIM:612016,
  • SCAR9,
  • coenzyme Q10 deficiency, primary, 4,
  • ORDO:139485,
  • COQ10D4
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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