OBO ID: DOID:0070240
Term Name: primary coenzyme Q10 deficiency 3 Search Ontology:
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 primary coenzyme Q10 deficiency 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PDSS2 Coenzyme Q10 deficiency, primary, 3 614652
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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