A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS2 gene on chromosome 6q21. [ url:https://www.ncbi.nlm.nih.gov/pubmed/17186472 http://purl.obolibrary.org/obo/ECO_0007645 ]

Synonyms: coenzyme Q10 deficiency, primary, 3 COQ10D3

This is just here as a test because I lose it

Term information

acronym
COQ10D3

has obo namespace

disease_ontology

id

DOID:0070240