Disease association ontology term - MONDO:0008133 - optic atrophy 3
Term summary
ID
MONDO:0008133
Name
optic atrophy 3
Ontology or CV name
Disease association
Parents
is_a
mitochondrial oxidative phosphorylation disorder
is_a
autosomal dominant optic atrophy
Annotation
Disease association
MONDO:0008133
-
optic atrophy 3
References:
PB_REF:0000006
Genes:
opa3 (SPBC1703.11)