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DOID:0070240 - primary coenzyme Q10 deficiency 3
Disease Ontology Definition:A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS2 gene on chromosome 6q21.
Synonyms: COQ10D3, coenzyme Q10 deficiency, primary, 3,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
coenzyme Q10 deficiency disease (is_a)