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: 7
- Hematologic Diseases: 3445
  - Hemorrhagic Disorders: 706
    - Hemophilia A: 11090
  - Blood Coagulation Disorders: 168
    - Inherited Blood Coagulation Disorders: 76
      - Hemophilia A: 11090
    - Coagulation Protein Disorders: 1
      - Hemophilia A: 11090
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inherited Blood Coagulation Disorders: 76
    - Hemophilia A: 11090

Bülent Zulfikar Selected Research

Bülent Zulfikar Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure