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Disease Ontology Browser
Worth syndrome (DOID:0080037)
Alliance: disease page
Synonyms: autosomal dominant endosteal hyperostosis; autosomal dominant osteosclerosis; benign form of Worth hyperostosis corticalis generalisata with torus platinus; Worth's syndrome
Alt IDs: OMIM:144750, MESH:C536748, ORDO:2790, UMLS_CUI:C0432273
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory