Worth syndrome

Summary
Synonym
  • Worth's syndrome
  • autosomal dominant endosteal hyperostosis
  • autosomal dominant osteosclerosis
  • benign form of Worth hyperostosis corticalis generalisata with torus platinus
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.
Super Class
autosomal dominant disease hyperostosis
Disease Ontology
DOID:0080037
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4041 LRP5 LDL receptor related protein 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
16973 Lrp5 low density lipoprotein receptor-related protein 5

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024