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Disease Ontology Browser
primary coenzyme Q10 deficiency 8 (DOID:0070245)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 8; COQ10D8
Alt IDs: OMIM:616733
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory