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Disease Ontology Browser
primary coenzyme Q10 deficiency 3 (DOID:0070240)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 3; COQ10D3
Alt IDs: OMIM:614652
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS2 gene on chromosome 6q21.

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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory