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Disease association ontology term - MONDO:0033656 - mitochondrial complex IV deficiency, nuclear type 21

Term summary

ID
MONDO:0033656
Name
mitochondrial complex IV deficiency, nuclear type 21
Ontology or CV name
Disease association
Definition
Any mitochondrial complex IV deficiency in which the cause of the disease is a mutation in the COXFA4 gene.

Parents

Annotation

Disease association

MONDO:0033656 - mitochondrial complex IV deficiency, nuclear type 21

References:

Genes: