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DO Term : Worth syndrome [DOID:0080037] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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:
OMIM:144750,
MESH:C536748,
Worth's syndrome,
benign form of Worth hyperostosis corticalis generalisata with torus platinus,
ORDO:2790,
GARD:390,
DOID:0111372,
UMLS_CUI:C0432273,
SNOMEDCT_US_2023_03_01:254131007,
autosomal dominant osteosclerosis,
144750,
autosomal dominant endosteal hyperostosis

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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