Disease association ontology term - MONDO:0020727 - combined oxidative phosphorylation deficiency 22

Term summary

ID: MONDO:0020727
Name: combined oxidative phosphorylation deficiency 22
Ontology or CV name: Disease association

Parents

is_a mitochondrial proton-transporting ATP synthase complex deficiency

Annotation

Disease association

MONDO:0020727 - combined oxidative phosphorylation deficiency 22

References:

PB_REF:0000006

Genes:

atp1 (SPAC14C4.14)