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autosomal dominant endosteal hyperostosis (DOID:0111372)
Alliance: disease page
Synonyms: Autosomal dominant osteosclerosis, Worth type; endosteal hyperostosis, Worth type; hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
Alt IDs: OMIM:144750, MESH:C536748, ORDO:2790, UMLS_CUI:C0432273
Definition: An osteosclerosis characterized by benign and usually asymptomatic osteosclerosis that is not associated with an increased fracture risk and craniofacial anomalies that has_material_basis_in heterozygous mutation in LRP5 on chromosome 11q13.2.


Contributing Projects:
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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last database update
03/24/2020
MGI 6.15
The Jackson Laboratory