Disease association ontology term - MONDO:0012543 - optic atrophy 5
Term summary
ID
MONDO:0012543
Name
optic atrophy 5
Ontology or CV name
Disease association
Parents
is_a
autosomal dominant optic atrophy
Annotation
Disease association
MONDO:0012543
-
optic atrophy 5
References:
PB_REF:0000006
Genes:
dnm1 (SPBC12C2.08)
vps1 (SPAC767.01c)