Worth's syndrome (Q8037184)

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hyperostosis that has material basis in a mutation in the LRP5 gene which results in increased bone density and bony structures located in palate
  • autosomal dominant endosteal hyperostosis
  • autosomal dominant osteosclerosis
  • benign form of Worth hyperostosis corticalis generalisata with torus platinus
  • Worth syndrome
  • obsolete autosomal dominant endosteal hyperostosis
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Language Label Description Also known as
English
Worth's syndrome
hyperostosis that has material basis in a mutation in the LRP5 gene which results in increased bone density and bony structures located in palate
  • autosomal dominant endosteal hyperostosis
  • autosomal dominant osteosclerosis
  • benign form of Worth hyperostosis corticalis generalisata with torus platinus
  • Worth syndrome
  • obsolete autosomal dominant endosteal hyperostosis

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