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Disease association ontology term - MONDO:0014356 - mitochondrial complex III deficiency nuclear type 7

Term summary

ID
MONDO:0014356
Name
mitochondrial complex III deficiency nuclear type 7
Ontology or CV name
Disease association
Definition
Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC2 gene.

Parents

Annotation

Disease association

MONDO:0014356 - mitochondrial complex III deficiency nuclear type 7

References:

Genes: