Disease association ontology term - MONDO:0030007 - combined oxidative phosphorylation deficiency 41

Term summary

ID: MONDO:0030007
Name: combined oxidative phosphorylation deficiency 41
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0030007 - combined oxidative phosphorylation deficiency 41

References:

PB_REF:0000006

Genes:

gta2 (SPAC343.13)