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Disease association ontology term - MONDO:0013838 - coenzyme Q10 deficiency, primary, 3

Term summary

ID
MONDO:0013838
Name
coenzyme Q10 deficiency, primary, 3
Ontology or CV name
Disease association
Definition
Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the PDSS2 gene.

Parents

Annotation

Disease association

MONDO:0013838 - coenzyme Q10 deficiency, primary, 3

References:

Genes: