has material basis in germline mutation in PDE6A inherited retinal dystrophy PDE6A-related retinopathy https://github.com/monarch-initiative/mondo/issues/6562 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/) PDE6A-related retinopathy MONDO:0700224 Any retinopathy caused by variants in the PDE6A gene. GARD:0026376