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Disease association ontology term - MONDO:0014066 - mitochondrial complex III deficiency nuclear type 5

Term summary

ID
MONDO:0014066
Name
mitochondrial complex III deficiency nuclear type 5
Ontology or CV name
Disease association
Definition
Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCRC2 gene.

Parents

Annotation

Disease association

MONDO:0014066 - mitochondrial complex III deficiency nuclear type 5

References:

Genes: