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Hemoglobin C Disease

A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
Also Known As:
Hemoglobin-C Disease; C Disease, Hemoglobin; C Diseases, Hemoglobin; Hemoglobin C Diseases; Hemoglobin-C Diseases
Networked: 20 relevant articles (0 outcomes, 4 trials/studies)

Disease Context: Research Results

Related Diseases

1. Sickle Cell Anemia (Hemoglobin S Disease)
2. Hemoglobinopathies
3. beta-Thalassemia (Cooley's Anemia)
4. Thalassemia
5. Anemia

Experts

1. Ault, Bettina H: 1 article (12/2009)
2. Sanders, John T: 1 article (12/2009)
3. Spencer, John David: 1 article (12/2009)
4. Nagababu, Enika: 1 article (07/2008)
5. Fabry, Mary E: 1 article (07/2008)
6. Rifkind, Joseph M: 1 article (07/2008)
7. Nagel, Ronald L: 1 article (07/2008)
8. Lee, H E: 1 article (11/2003)
9. Marder, V J: 1 article (11/2003)
10. Miller, B J: 1 article (11/2003)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Hemoglobin C Disease:
1. Hemoglobins (Hemoglobin)IBA
2. Hemoglobin CIBA
3. beta-Globins (beta Globin)IBA
4. CopperIBA
5. Hemoglobin AIBA
6. Sickle HemoglobinIBA
7. Pyruvate KinaseIBA
8. IronIBA
9. Heme (Haem)IBA
10. Fetal Hemoglobin (Hemoglobin F)IBA

Therapies and Procedures

1. Splenectomy