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. The disease is nevoid basal cell carcinoma syndrome (MONDO_0007187, a Monarch Disease Ontology identifier). Also known as: Gorlin syndrome, Gorlin-Goltz syndrome, NBCCS, basal cell nevus syndrome, multiple basal cell carcinomas, nevoid basal cell cancer syndrome.