primary coenzyme Q10 deficiency 6 Disease Ontology Browser

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Disease Ontology Browser

primary coenzyme Q10 deficiency 6 (DOID:0070243)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 6; COQ10D6; familial steroid-resistant nephrotic syndrome with sensorineural deafness
Alt IDs: OMIM:614650, ORDO:280406
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ6 gene on chromosome 14q24.3.

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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