Disease association ontology term - MONDO:0030017 - combined oxidative phosphorylation deficiency 43

Term summary

ID: MONDO:0030017
Name: combined oxidative phosphorylation deficiency 43
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0030017 - combined oxidative phosphorylation deficiency 43

References:

PB_REF:0000006

Genes:

tim22 (SPBC25H2.04c)