disease has feature autosomal dominant disease nevoid basal cell carcinoma syndrome https://www.malacards.org/card/basal_cell_nevus_syndrome_1 MESH:D001478 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. NANDO:2200828 DOID:2512 NORD:1507 Gorlin syndrome MONDO:0007187 UMLS:C0004779 BCNS MEDGEN:2554 nevoid basal cell cancer syndrome basal cell nevus syndrome NBCCS icd11.foundation:1012745138 Gorlin-Goltz syndrome Orphanet:377 DOID:0070365 GARD:0007166 nevoid basal cell carcinoma syndrome MedDRA:10062804 OMIMPS:109400 NCIT:C2892 multiple basal cell carcinomas SCTID:69408002 hereditary neoplastic syndrome developmental defect during embryogenesis eyelid cancer neurocutaneous syndrome hereditary neurological disease