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MeSH 搜索器

Gardner Syndrome

A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract.
推出的年份: 1981
副标题
树号: C04.557.470.035.215.100.500, C04.588.274.476.411.307.089.393, C04.700.100.392, C06.301.371.411.307.090.500, C06.405.249.411.307.090.500, C06.405.469.158.356.090.500, C06.405.469.491.307.090.500, C06.405.469.578.249.393, C16.131.077.393, C16.320.700.100.393
MeSH 单一 ID: D005736
进入的组:
  • Gardner Syndromes
  • Syndrome, Gardner
  • Syndromes, Gardner
  • Gardner's Syndrome
  • Gardner's Syndromes
  • Gardners Syndrome
  • Syndrome, Gardner's
  • Syndromes, Gardner's
早前的内容:
  • Colonic Neoplasms (1966-1980)
  • Intestinal Polyps/FG (1968-1980)
  • Neoplasms, Multiple Primary (1966-1980)

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