hereditary multiple exostoses (Q1952467)

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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
Language Label Description Also known as
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

instance of
rare disease
0 references
class of disease
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Commons category
Hereditary multiple exostoses
0 references

Identifiers

KEGG ID
H00122
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ICD-9 ID
756.59
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Mondo ID
MONDO_0005508
0 references
 
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