Disease association ontology term - MONDO:0032869 - mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6

Term summary

ID: MONDO:0032869
Name: mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6
Ontology or CV name: Disease association

Parents

is_a mitochondrial proton-transporting ATP synthase complex deficiency

Annotation

Disease association

MONDO:0032869 - mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6

References:

Genes:

atp19 (SPAC25H1.10c)