PomBase home

Disease association ontology term - MONDO:0033655 - mitochondrial complex IV deficiency, nuclear type 20

Term summary

ID
MONDO:0033655
Name
mitochondrial complex IV deficiency, nuclear type 20
Ontology or CV name
Disease association
Definition
Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX5A gene.

Parents

Annotation

Disease association

MONDO:0033655 - mitochondrial complex IV deficiency, nuclear type 20

References:

Genes: