FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Worth syndrome ID (Ontology) DOID:0080037 (Human Disease)
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.
Also Known As "autosomal dominant endosteal hyperostosis" ; "autosomal dominant osteosclerosis" ; "benign form of Worth hyperostosis corticalis generalisata with torus platinus" (for all, see Synonyms field below)
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 Genes
 Worth syndrome       2
 for disease ribbon | Worth syndrome       2
 model of | Worth syndrome       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
bone remodeling disease         |
 |__hyperostosis________________|
                                Worth syndrome  2 rec.
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Is a autosomal dominant disease
hyperostosis
Part of
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Synonyms
  • "autosomal dominant endosteal hyperostosis" EXACT
    "autosomal dominant osteosclerosis" EXACT
    "benign form of Worth hyperostosis corticalis generalisata with torus platinus" EXACT
    "Worth's syndrome" EXACT
Secondary IDs
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GARD:390
MESH:C536748
MIM:144750
ORDO:2790
SNOMEDCT_US_2023_03_01:254131007
UMLS_CUI:C0432273