Human genes for primary coenzyme Q10 deficiency 6
Primary coenzyme Q10 deficiency 6 [DOID:0070243]
A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of COQ6 on chromosome 14q24.3.
Synonyms: primary coenzyme Q10 deficiency 6, DOID:0070243, coenzyme Q10 deficiency, primary, 6, COQ10D6, familial steroid-resistant nephrotic syndrome with sensorineural deafness ...