Disease association ontology term - MONDO:0030311 - combined oxidative phosphorylation deficiency 52

Term summary

ID: MONDO:0030311
Name: combined oxidative phosphorylation deficiency 52
Ontology or CV name: Disease association

Parents

is_a combined oxidative phosphorylation deficiency

Annotation

Disease association

MONDO:0030311 - combined oxidative phosphorylation deficiency 52

References:

PB_REF:0000006

Genes:

nfs1 (SPBC21D10.11c)