Disease association ontology term - MONDO:0030008 - combined oxidative phosphorylation deficiency 42

Term summary

ID: MONDO:0030008
Name: combined oxidative phosphorylation deficiency 42
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0030008 - combined oxidative phosphorylation deficiency 42

References:

PB_REF:0000006

Genes:

gta3 (SPCC777.11)