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Disease association ontology term - MONDO:0014547 - combined oxidative phosphorylation defect type 24

Term summary

ID
MONDO:0014547
Name
combined oxidative phosphorylation defect type 24
Ontology or CV name
Disease association
Definition
Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the NARS2 gene.

Parents

Annotation

Disease association

MONDO:0014547 - combined oxidative phosphorylation defect type 24

References:

Genes: