(Q1952467)

English

hereditary multiple exostoses

exostosis that has material basis in a mutation on the genes EXT1, EXT2 and EXT3 which results in multiple bony spurs throughout a child's growth

  • Multiple congenital exostosis
  • Multiple exostosis syndromes
  • Osteochondromatosis syndrome (disorder) [Ambiguous]
  • hereditary multiple exostoses 1
  • hereditary multiple exostoses 2
  • hereditary multiple exostoses 3
  • multiple ostechondromas
  • Osteochondromatosis syndrome
  • HMO
  • Bessel-Hagen disease
  • Multiple cartilaginous exostoses
  • Multiple exostoses
  • Hereditary multiple exostosis
  • Hereditary multiple exostoses
  • exostoses, multiple

Statements

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Hereditary multiple exostoses
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Identifiers

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