A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ7 gene on chromosome 16p12.3. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/26084283 ]

Synonyms: COQ10D8 coenzyme Q10 deficiency, primary, 8

This is just here as a test because I lose it

Term information

acronym
COQ10D8

has obo namespace

disease_ontology

id

DOID:0070245