DISEASES

Disease-gene associations mined from literature

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 ...