CERKL-related retinopathy
http://purl.obolibrary.org/obo/MONDO_0800401
An inherited retinopathy caused by bi-allelic variants in the CERKL gene. [ MONDO:patterns/disease_series_by_gene https://clinicalgenome.org/affiliation/40072/ ]
Term info
https://github.com/monarch-initiative/mondo/issues/5693
An inherited retinopathy caused by bi-allelic variants in the CERKL gene.
MONDO:0800401