Disease association ontology term - MONDO:0700227 - ELOVL4-related maculopathy
Term summary
ID
MONDO:0700227
Name
ELOVL4-related maculopathy
Ontology or CV name
Disease association
Definition
Any maculopathy caused by a variant in the ELOVL4 gene.
Parents
is_a
inherited retinal dystrophy
Annotation
Disease association
MONDO:0010819
-
Stargardt disease 3
References:
PB_REF:0000006
Genes:
elo1 (SPAC1639.01c)
elo2 (SPAC1B2.03c)