Disease association ontology term - MONDO:0957992 - combined oxidative phosphorylation deficiency 59

Term summary

ID: MONDO:0957992
Name: combined oxidative phosphorylation deficiency 59
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0957992 - combined oxidative phosphorylation deficiency 59

References:

PB_REF:0000006

Genes:

mrpl51 (SPBC19C2.12)