Sickle Cell Anemia

A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.

Also Known As:

Hemoglobin S Disease; Anemia, Sickle Cell; HbS Disease; Sickle Cell Disease; Sickle Cell Disorders; Sickling Disorder Due to Hemoglobin S; Anemias, Sickle Cell; Cell Disease, Sickle; Cell Diseases, Sickle; Cell Disorder, Sickle; Cell Disorders, Sickle; Disease, Hemoglobin S; Hemoglobin S Diseases; Sickle Cell Anemias; Sickle Cell Diseases; Sickle Cell Disorder

Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Anemia: 38331
    - Hemolytic Anemia: 6695
      - Congenital Hemolytic Anemia: 288
        Sickle Cell Anemia: 9866
  - Hemoglobinopathies: 2001
    - Sickle Cell Anemia: 9866
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hemoglobinopathies: 2001
    - Sickle Cell Anemia: 9866
  - Congenital Hemolytic Anemia: 288
    - Sickle Cell Anemia: 9866

Mark Roosjen Selected Research

Mark Roosjen Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure