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primary coenzyme Q10 deficiency 5 (DOID:0070242)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 5; COQ10D5; encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Alt IDs: OMIM:614654, ORDO:319678
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ9 gene on chromosome 16q21.

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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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11/19/2024
MGI 6.24 		The Jackson Laboratory