MeSH 搜索器

Osteogenesis Imperfecta

COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I.
推出的年份:
副标题
树号: C05.116.099.708.685, C16.320.737, C17.300.200.540
MeSH 单一 ID: D010013
进入的组:
  • Brittle Bone Disease
  • Fragilitas Ossium
  • Ossiums, Fragilitas
  • Lobstein's Disease
  • Disease, Lobstein's
  • Lobsteins Disease
  • Osteogenesis Imperfecta, Type I
  • Osteogenesis Imperfecta with Blue Sclerae
  • Osteogenesis Imperfecta, Type 1
  • Lobstein Disease
  • Disease, Lobstein
  • Osteogenesis Imperfecta Tarda
  • Osteogenesis Imperfecta Tardas

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