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Disease association ontology term - MONDO:0020858 - mitochondrial complex V (ATP synthase) deficiency, nuclear type 5

Term summary

ID
MONDO:0020858
Name
mitochondrial complex V (ATP synthase) deficiency, nuclear type 5
Ontology or CV name
Disease association
Definition
Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the ATP5F1D gene.

Parents

Annotation

Disease association

MONDO:0020858 - mitochondrial complex V (ATP synthase) deficiency, nuclear type 5

References:

Genes: