Disease association ontology term - MONDO:0957935 - optic atrophy 15
Term summary
ID
MONDO:0957935
Name
optic atrophy 15
Ontology or CV name
Disease association
Parents
is_a
hereditary optic atrophy
Annotation
Disease association
MONDO:0957935
-
optic atrophy 15
References:
PB_REF:0000006
Genes:
mct1 (SPAC11G7.05c)