_:vb50939973 . . _:vb50939973 . . "COQ10D5"@en . "primary coenzyme Q10 deficiency 5"^^ . "coenzyme Q10 deficiency, primary, 5"@en . _:vb50939973 . "OMIM:614654"^^ . _:vb50939973 . "encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome"@en . "A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of COQ9 on chromosome 16q21."^^ . . _:vb50939973 . "ORDO:319678"^^ . "DOID:0070242"^^ . "disease_ontology"^^ .