Term Name:	primary coenzyme Q10 deficiency 7
Synonyms:	coenzyme Q10 deficiency, primary, 7, COQ10D7, COQ4-related neonatal encephalomyopathy, neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
Definition:	A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ4 gene on chromosome 9q34.11.
Ontology:	Human Disease [DOID:0070244]   ( DOID:0070244 )