Afibrinogenemia

A deficiency or absence of FIBRINOGEN in the blood.

Also Known As:

Fibrinogen Deficiency; Afibrinogenemia, Congenital; Congenital Afibrinogenaemia; Congenital Afibrinogenemia; Deficiency, Fibrinogen; Familial Afibrinogenemia; Hypofibrinogenemia, Congenital; Afibrinogenaemia, Congenital; Afibrinogenaemias, Congenital; Afibrinogenemia, Familial; Afibrinogenemias; Afibrinogenemias, Congenital; Afibrinogenemias, Familial; Congenital Afibrinogenaemias; Congenital Afibrinogenemias; Congenital Hypofibrinogenemia; Congenital Hypofibrinogenemias; Familial Afibrinogenemias; Fibrinogen Deficiencies; Hypofibrinogenemias, Congenital

Hemic and Lymphatic Diseases: 7
- Hematologic Diseases: 3445
  - Hemorrhagic Disorders: 706
    - Afibrinogenemia: 440
  - Blood Coagulation Disorders: 168
    - Inherited Blood Coagulation Disorders: 76
      - Afibrinogenemia: 440
    - Coagulation Protein Disorders: 1
      - Afibrinogenemia: 440
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inherited Blood Coagulation Disorders: 76
    - Afibrinogenemia: 440

B Padrazzi Selected Research

B Padrazzi Research Topics

Disease

Drug/Important Bio-Agent (IBA)