Any maculopathy caused by a variant in the ELOVL4 gene. [ https://clinicalgenome.org/working-groups/clinical-domain/ocular-cdwg/ ]
Synonyms: ELOVL4-related maculopathy
Term information
rare, inferred_rare
This term captures the disease spectrum. At the time of creation (January 2024), this term is the ontological parent to only one term, but other clinical disease terms could be added in the future. If no additional ontological children are discovered, it is possible that this term might be merged with its single child. (https://clinicalgenome.org/working-groups/clinical-domain/ocular-cdwg/)