Summary Literature (0)

DOID:0080037 - Worth's 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, autosomal dominant endosteal hyperostosis, autosomal dominant osteosclerosis, benign form of Worth hyperostosis corticalis generalisata with torus platinus,

Echinobase Genes :


OMIM:

MIM:607636 - van buchem disease, type 2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee