MeSH 搜索器

Factor X Deficiency

Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
推出的年份: 1991(1975)
副标题
树号: C15.378.100.100.320, C15.378.100.141.320, C15.378.463.320, C16.320.099.320
MeSH 单一 ID: D005171
进入的组:
  • Deficiency, Factor Ten
  • Deficiencies, Factor Ten
  • Factor Ten Deficiencies
  • Ten Deficiencies, Factor
  • Factor 10 Deficiency
  • Factor Ten Deficiency
  • Stuart-Prower Factor Deficiency
  • Stuart Prower Factor Deficiency
  • Deficiency, Stuart-Prower
  • Deficiency, Stuart Prower
  • Stuart-Prower Deficiency
  • Stuart Prower Deficiency
  • Deficiency, Stuart-Prower Factor
  • Deficiency, Stuart Prower Factor
  • Deficiency, Factor 10
  • Deficiencies, Factor 10
  • Factor 10 Deficiencies
  • Deficiency, Factor X
  • Deficiencies, Factor X
  • Factor X Deficiencies

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