Disease association ontology term - MONDO:0033537 - combined oxidative phosphorylation deficiency 47

Term summary

ID: MONDO:0033537
Name: combined oxidative phosphorylation deficiency 47
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0033537 - combined oxidative phosphorylation deficiency 47

References:

PB_REF:0000006

Genes:

mrp51 (SPAC23A1.18c)