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D005171Level 6

Factor X Deficiency

**Definition:** 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.

**Tree numbers:** - C15.378.100.100.320 - C15.378.100.141.320 - C15.378.463.320 - C16.320.099.320

**Synonyms:** - Deficiency, Factor Ten - Factor 10 Deficiency - Factor Ten Deficiency - Deficiency, Factor X - Deficiency, Stuart-Prower - Stuart-Prower Deficiency - Deficiency, Stuart-Prower Factor - Deficiency, Factor 10 - Stuart-Prower Factor Deficiency

GET/api/v1/systems/mesh/nodes/D005171
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