BabelNet

bn:01503113n

Noun Concept

Categories: Congenital disorders, Syndromes, Rare diseases, Autosomal dominant disorders

Worth syndrome Worth's syndrome autosomal dominant endosteal hyperostosis autosomal dominant osteosclerosis benign form of Worth hyperostosis corticalis generalisata with torus platinus

Worth syndrome, also known as benign form of Worth hyperostosis corticalis generalisata with torus platinus, autosomal dominant osteosclerosis, autosomal dominant endosteal hyperostosis or Worth disease, is a rare autosomal dominant congenital disorder that is caused by a mutation in the LRP5 gene. Wikipedia

Definitions

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Genetic disorder Wikipedia Disambiguation

Hyperostosis that has material basis in a mutation in the LRP5 gene which results in increased bone density and bony structures located in palate Wikidata

IS A

rare disease

genetic disease

hyperostosis

cortical hyperostosis

GENETIC ASSOCIATION

LRP5

HAS PHENOTYPE

osteosclerosis

hyperostosis

Wikipedia

Worth syndrome