obsolete_Gorlin syndrome true multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies SCTID:69408002 MESH:D001478 Replaced with Mondo term. Orphanet:377 OMIM:109400 NCIT:C2892 A rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities. ICD10:Q87.8 NBCCS nevoid basal cell cancer syndrome GARD:0007166 nevoid basal cell carcinoma syndrome MedDRA:10062804 Gorlin-Goltz syndrome BCNS multiple basal cell carcinomas UMLS:C0004779 basal cell nevus syndrome 3.41.0 http://purl.obolibrary.org/obo/MONDO_0007187 DOID:2512 Gorlin syndrome