Term Name: primary coenzyme Q10 deficiency 8
Synonyms: coenzyme Q10 deficiency, primary, 8, COQ10D8
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3.
Ontology: Human Disease [DOID:0070245]   ( DOID:0070245 )

Relationships
is a type of: coenzyme Q10 deficiency disease