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Disease Ontology Browser
primary coenzyme Q10 deficiency 7 (DOID:0070244)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 7; COQ4-related neonatal encephalomyopathy; COQ10D7; neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
Alt IDs: OMIM:616276, ORDO:457185
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ4 gene on chromosome 9q34.11.

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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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11/12/2024
MGI 6.24 		The Jackson Laboratory