has characteristic has characteristic has material basis in germline mutation in IMPG1 Autosomal recessive inheritance autosomal recessive disease inherited retinal dystrophy IMPG1-related recessive retinopathy https://github.com/monarch-initiative/mondo/issues/7923 GARD:0027240 Any retinopathy caused by autosomal recessive variants in the IMPG1 gene. This term captures the disease spectrum. At the time of creation (September 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/) MONDO:1040037 IMPG1-related recessive retinopathy