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Disease association ontology term - MONDO:0014091 - mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B

Term summary

ID
MONDO:0014091
Name
mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B
Ontology or CV name
Disease association
Definition
Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the ATP5F1A gene.

Parents

Annotation

Disease association

MONDO:0014091 - mitochondrial complex V (ATP synthase) deficiency, nuclear type 4B

References:

Genes: