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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)
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12/10/2024
MGI 6.24 		The Jackson Laboratory