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: 6
- Hematologic Diseases: 3366
  - Hemorrhagic Disorders: 702
    - Afibrinogenemia: 436
  - Blood Coagulation Disorders: 167
    - Inherited Blood Coagulation Disorders: 74
      - Afibrinogenemia: 436
    - Coagulation Protein Disorders: 1
      - Afibrinogenemia: 436
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inherited Blood Coagulation Disorders: 74
    - Afibrinogenemia: 436

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Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure