Search Ontology:
Human Disease

Worth syndrome

Term ID
DOID:0080037
Synonyms
  • autosomal dominant endosteal hyperostosis
  • autosomal dominant osteosclerosis
  • benign form of Worth hyperostosis corticalis generalisata with torus platinus
  • Worth's syndrome
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. (4)
References
Ontology
Human Disease   ( DOID:0080037 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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