Disease association ontology term - MONDO:0032726 - combined oxidative phosphorylation deficiency 39

Term summary

ID: MONDO:0032726
Name: combined oxidative phosphorylation deficiency 39
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0032726 - combined oxidative phosphorylation deficiency 39

References:

PB_REF:0000006

Genes:

gfm2 (SPBC660.10)