About   Help   FAQ
Disease Ontology Browser
primary coenzyme Q10 deficiency 1 (DOID:0070238)
Alliance: disease page
Synonyms: coenzyme Q deficiency 1; CoQ10 deficiency, primary, 1; COQ10D1; CoQ deficiency 1; ubiquinone deficiency 1
Alt IDs: OMIM:607426
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ2 gene on chromosome 4q21.22-q21.23.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory