has material basis in germline mutation in BBS10 ciliopathy BBS10-related ciliopathy https://github.com/monarch-initiative/mondo/issues/6562 MONDO:0700237 GARD:0026386 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/) BBS10-related ciliopathy Any ciliopathy caused by variants in the BBS10 gene.