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.

Also Known As:

Deficiency, Factor 10; Deficiency, Factor Ten; Deficiency, Factor X; Deficiency, Stuart-Prower; Deficiency, Stuart-Prower Factor; Factor 10 Deficiency; Factor Ten Deficiency; Stuart-Prower Deficiency; Stuart-Prower Factor Deficiency; Deficiencies, Factor 10; Deficiencies, Factor Ten; Deficiencies, Factor X; Deficiency, Stuart Prower; Deficiency, Stuart Prower Factor; Factor 10 Deficiencies; Factor Ten Deficiencies; Factor X Deficiencies; Stuart Prower Deficiency; Stuart Prower Factor Deficiency; Ten Deficiencies, Factor

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Hemorrhagic Disorders: 706
    - Factor X Deficiency: 198
  - Blood Coagulation Disorders: 168
    - Inherited Blood Coagulation Disorders: 76
      - Factor X Deficiency: 198
    - Coagulation Protein Disorders: 1
      - Factor X Deficiency: 198
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inherited Blood Coagulation Disorders: 76
    - Factor X Deficiency: 198

Ghufran Alofi Selected Research

Ghufran Alofi Research Topics

Disease

Drug/Important Bio-Agent (IBA)