Term Name: Worth syndrome
Synonyms: autosomal dominant endosteal hyperostosis, autosomal dominant osteosclerosis, benign form of Worth hyperostosis corticalis generalisata with torus platinus, Worth's syndrome
Definition: A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate.
Ontology: Human Disease [DOID:0080037]   ( DOID:0080037 )

Relationships
is a type of: autosomal dominant disease hyperostosis