primary coenzyme Q10 deficiency 7 (DOID:0070244)
Alliance: disease page
Synonyms: coenzyme Q10 deficiency, primary, 7; COQ4-related neonatal encephalomyopathy; COQ10D7; neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
Alt IDs: OMIM:616276, ORDO:457185
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ4 gene on chromosome 9q34.11.