Disease association ontology term - MONDO:0014571 - optic atrophy 9
Term summary
ID
MONDO:0014571
Name
optic atrophy 9
Ontology or CV name
Disease association
Parents
is_a
ACO2-related optic atrophy with or without extraocular features
Annotation
Disease association
MONDO:0014571
-
optic atrophy 9
References:
PB_REF:0000006
Genes:
aco1 (SPAC24C9.06c)
aco2 (SPBP4H10.15)