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Disease • C0015519
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 consump
Synonyms
Factor X Deficiency • Deficiency, factor X • Deficiencies, Factor X • Factor X Deficiencies • Stuart-Prower Deficiency • Stuart Prower Deficiency • Deficiency, Stuart Prower • Deficiency, Stuart-Prower • Stuart-Prower Factor Deficiency • Stuart Prower Factor Deficiency • Deficiency, Stuart Prower Factor • Deficiency, Stuart-Prower Factor • Disease, Stuart-Prower • DEFIC FACTOR X • FACTOR X DEFIC • DEFIC STUART PROWER • STUART PROWER DEFIC • DEFIC STUART PROWER FACTOR • STUART PROWER FACTOR DEFIC • Factor X Deficiency [Disease/Finding]
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F10 gene
Hemorrhagic Disorders
Blood Coagulation Disorders, Inherited
Coagulation Protein Disorders
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