Disease association ontology term - MONDO:0032712 - combined oxidative phosphorylation deficiency 38

Term summary

ID: MONDO:0032712
Name: combined oxidative phosphorylation deficiency 38
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0032712 - combined oxidative phosphorylation deficiency 38

References:

PB_REF:0000006

Genes:

mrp2 (SPAC23H3.07c)