Term Name:	primary coenzyme Q10 deficiency 4
Synonyms:	coenzyme Q10 deficiency, primary, 4, COQ10D4, SCAR9, spinocerebellar ataxia, autosomal recessive 9
Definition:	A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the ADCK3 gene on chromosome 1q42.13.
Ontology:	Human Disease [DOID:0070241]   ( DOID:0070241 )