FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term primary coenzyme Q10 deficiency 8 ID (Ontology) DOID:0070245 (Human Disease)
Definition A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3.
Also Known As "coenzyme Q10 deficiency, primary, 8" ; "COQ10D8"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 primary coenzyme Q10 deficiency 8       1
 for disease ribbon | primary coenzyme Q10 deficiency 8       1
 model of | primary coenzyme Q10 deficiency 8       1
Spanning Tree (Parents/Children)
Only view relationship: 
  mitochondrial metabolism disease
   |__coenzyme Q10 deficiency disease
       |__primary coenzyme Q10 deficiency 8  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a coenzyme Q10 deficiency disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "coenzyme Q10 deficiency, primary, 8" EXACT
    "COQ10D8" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MIM:616733