"32107" . "2790"^^ . . . . . "Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate."@en . . "Q78.2" . . . . . . . . "2790" . . . "Worth syndrome has an autosomal dominant pattern of inheritance."@en . . . . . . "Worth syndrome"@en . . "144750"^^ . . . . . . . . . . "3407"^^ . . . . . . "Worth syndrome"@en . "1046811874"^^ . . . . . . . . . . . . . . "144750"^^ . "32107"^^ . . . . . . . . . . . . . . "Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate."@en . . . . . . "Worth syndrome"@en . . . "Q78.2"@en . . . . "22068733"^^ .