Summary Literature (0)

DOID:0080037 - Worth syndrome

Disease Ontology 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.

Synonyms: autosomal dominant endosteal hyperostosis, autosomal dominant osteosclerosis, benign form of Worth hyperostosis corticalis generalisata with torus platinus, Worth's syndrome, Worth syndrome

Xenbase Genes : lrp5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011878 - Worth syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee