PomBase home

Disease association ontology term - MONDO:0011829 - coenzyme Q10 deficiency, primary, 1

Term summary

ID
MONDO:0011829
Name
coenzyme Q10 deficiency, primary, 1
Ontology or CV name
Disease association
Definition
Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ2 gene.

Parents

Annotation

Disease association

MONDO:0011829 - coenzyme Q10 deficiency, primary, 1

References:

Genes: