JSON

CNGB1-related retinopathy

^ http://purl.obolibrary.org/obo/MONDO_0800403

An inherited retinopathy caused by bi-allelic variants in the CNGB1 gene. [ MONDO:patterns/disease_series_by_gene https://clinicalgenome.org/affiliation/40072/ ]

Term info

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5693

definition

An inherited retinopathy caused by bi-allelic variants in the CNGB1 gene.

id

MONDO:0800403

Term relations