Hemophilia A

The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.

Also Known As:

Haemophilia; Hemophilia; Factor VIII Deficiency; Autosomal Hemophilia A; Classic Hemophilia; Deficiency, Factor VIII; Factor 8 Deficiency, Congenital; Factor VIII Deficiency, Congenital; Hemophilia A, Congenital; Hemophilia, Classic; As, Autosomal Hemophilia; Autosomal Hemophilia As; Classic Hemophilias; Congenital Hemophilia A; Congenital Hemophilia As; Hemophilia A, Autosomal; Hemophilia As; Hemophilia As, Autosomal; Hemophilia As, Congenital; Hemophilias, Classic

Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Hemorrhagic Disorders: 702
    - Hemophilia A: 10849
  - Blood Coagulation Disorders: 167
    - Inherited Blood Coagulation Disorders: 74
      - Hemophilia A: 10849
    - Coagulation Protein Disorders: 1
      - Hemophilia A: 10849
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inherited Blood Coagulation Disorders: 74
    - Hemophilia A: 10849

C Escuriola Ettingshausen Selected Research

C Escuriola Ettingshausen Research Topics

Disease

Drug/Important Bio-Agent (IBA)