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Disease association ontology term - MONDO:0859160 - mitochondrial complex IV deficiency, nuclear type 22

Term summary

ID
MONDO:0859160
Name
mitochondrial complex IV deficiency, nuclear type 22
Ontology or CV name
Disease association
Definition
Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COX16 gene.

Parents

Annotation

Disease association

MONDO:0859160 - mitochondrial complex IV deficiency, nuclear type 22

References:

Genes: