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Disease association ontology term - MONDO:0007415 - mitochondrial complex III deficiency nuclear type 1

Term summary

ID
MONDO:0007415
Name
mitochondrial complex III deficiency nuclear type 1
Ontology or CV name
Disease association
Definition
Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the BCS1L gene.

Parents

Annotation

Disease association

MONDO:0007415 - mitochondrial complex III deficiency nuclear type 1

References:

Genes: