Term Name: primary coenzyme Q10 deficiency 3
Synonyms: coenzyme Q10 deficiency, primary, 3, COQ10D3
Definition: A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS2 gene on chromosome 6q21.
Ontology: Human Disease [DOID:0070240]   ( DOID:0070240 )

Relationships
is a type of: coenzyme Q10 deficiency disease