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.
Year introduced: 1991(1975)
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Subheadings:
Tree Number(s): C15.378.100.100.320, C15.378.100.141.320, C15.378.463.320, C16.320.099.320
MeSH Unique ID: D005171
Entry Terms:
- Deficiency, Factor Ten
- Deficiencies, Factor Ten
- Factor Ten Deficiencies
- Ten Deficiencies, Factor
- Factor 10 Deficiency
- Factor Ten Deficiency
- Deficiency, Factor X
- Deficiencies, Factor X
- Factor X Deficiencies
- 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
- Stuart-Prower Factor Deficiency
- Stuart Prower Factor Deficiency