Search Ontology:
Human Disease

primary coenzyme Q10 deficiency 3

Term ID
DOID:0070240
Synonyms
  • coenzyme Q10 deficiency, primary, 3
  • COQ10D3
Definition
A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS2 gene on chromosome 6q21. https://www.ncbi.nlm.nih.gov/pubmed/17186472
References
Ontology
Human Disease   ( DOID:0070240 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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