search

MeSH 搜索器

Ehlers-Danlos Syndrome

A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.
推出的年份:
副标题
树号: C14.907.454.240, C15.378.463.515.240, C16.131.831.428, C16.320.850.260, C17.300.200.310, C17.800.804.428, C17.800.827.260
MeSH 单一 ID: D004535
进入的组:
  • Ehlers Danlos Syndrome
  • Syndrome, Ehlers-Danlos
  • Cutis Elastica
  • Ehlers Danlos Disease
  • Danlos Disease, Ehlers
  • Disease, Ehlers Danlos
  • Ehlers-Danlos Disease
  • Disease, Ehlers-Danlos
  • Ehlers-Danlos Syndrome, Type IV
  • Ehlers Danlos Syndrome, Type IV
  • Ehlers-Danlos Syndrome, Arterial Type
  • Ehlers-Danlos Syndrome, Ecchymotic Type
  • Ehlers-Danlos Syndrome, Sack-Barabas Type
  • Ehlers Danlos Syndrome, Sack-Barabas Type
  • Ehlers Danlos Syndrome, Sack Barabas Type
  • Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant
  • Ehlers Danlos Syndrome Type 4, Autosomal Dominant
  • Ehlers Danlos Syndrome, Arterial Type
  • Ehlers Danlos Syndrome, Ecchymotic Type
  • Ehlers-Danlos Syndrome, Vascular Type
  • Ehlers Danlos Syndrome, Vascular Type
  • EDS IV

留言 (0)

沒有登入
gif