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

In OMIM:
OMIM:144750 - ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT
OMIM:607636 - VAN BUCHEM DISEASE, TYPE 2

In Mondo Disease Ontology:
MONDO:0011878 - Worth syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : lrp5

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), hyperostosis (is_a)