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Disease association ontology term - MONDO:0033645 - mitochondrial complex IV deficiency, nuclear type 11

Term summary

ID
MONDO:0033645
Name
mitochondrial complex IV deficiency, nuclear type 11
Ontology or CV name
Disease association
Definition
Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX20 gene.

Parents

Annotation

Disease association

MONDO:0033645 - mitochondrial complex IV deficiency, nuclear type 11

References:

Genes: