MeSH 搜索器

Basal Cell Nevus Syndrome

Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
推出的年份: 1991(1980)
副标题
树号: C04.182.089.530.690.150, C04.557.470.200.165.150, C04.557.470.565.165.150, C04.700.175, C05.116.099.105, C05.500.470.690.150, C07.320.450.670.130, C16.131.077.130, C16.320.700.175
MeSH 单一 ID: D001478
进入的组:
  • Gorlin Syndrome
  • Syndrome, Gorlin
  • Gorlin-Goltz Syndrome
  • Gorlin Goltz Syndrome
  • Syndrome, Gorlin-Goltz
  • NBCCS
  • Nevoid Basal Cell Carcinoma Syndrome
  • Nevus Syndrome, Basal Cell
  • Fifth Phacomatosis
  • Fifth Phacomatoses
  • Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies
早前的内容:
  • Bone Cyst (1966-1979)
  • Carcinoma, Basal Cell (1966-1979)
  • Jaw Diseases (1967-1979)
  • Jaw Neoplasms (1967-1979)
  • Skin Neoplasms (1967-1979)
  • Syndrome (1972-1979)
  • specific jaw disease (1967-1979)
  • specific jaw neoplasm (1967-1979)

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