Human genes for primary coenzyme Q10 deficiency 5
Primary coenzyme Q10 deficiency 5 [DOID:0070242]
A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of COQ9 on chromosome 16q21.
Synonyms: primary coenzyme Q10 deficiency 5, DOID:0070242, coenzyme Q10 deficiency, primary, 5, COQ10D5, encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome ...