PomBase home

Disease association ontology term - MONDO:0014364 - mitochondrial complex III deficiency nuclear type 8

Term summary

ID
MONDO:0014364
Name
mitochondrial complex III deficiency nuclear type 8
Ontology or CV name
Disease association
Definition
Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the LYRM7 gene.

Parents

Annotation

Disease association

MONDO:0014364 - mitochondrial complex III deficiency nuclear type 8

References:

Genes: