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RP1-related recessive retinopathy

^ http://purl.obolibrary.org/obo/MONDO_0800399

An autosomal dominant retinopathy caused by variants in the RP1 gene. [ https://clinicalgenome.org/affiliation/40072/ MONDO:patterns/disease_series_by_gene ]

Term info

IAO 0000233

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

definition

An autosomal dominant retinopathy caused by variants in the RP1 gene.

id

MONDO:0800399