About   Help   FAQ
Disease Ontology Browser
primary coenzyme Q10 deficiency 4 (DOID:0070241)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 4; COQ10D4; SCAR9; spinocerebellar ataxia, autosomal recessive 9
Alt IDs: OMIM:612016, ORDO:139485
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the ADCK3 gene on chromosome 1q42.13.

Disease References using Mouse Models (1)
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
11/19/2024
MGI 6.24 		The Jackson Laboratory