Disease association ontology term - MONDO:0957978 - optic atrophy 16
Term summary
ID
MONDO:0957978
Name
optic atrophy 16
Ontology or CV name
Disease association
Parents
is_a
hereditary optic atrophy
Annotation
Disease association
MONDO:0957978
-
optic atrophy 16
References:
PB_REF:0000006
Genes:
etr1 (SPAC26F1.04c)