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.

Year introduced: 1972(1966)

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Tree Number(s): C15.378.050.141.150.490, C15.378.420.463, C16.320.070.490, C16.320.365.463

MeSH Unique ID: D006445

Entry Terms:

• C Disease, Hemoglobin
• C Diseases, Hemoglobin
• Hemoglobin C Diseases
• Hemoglobin-C Disease
• Hemoglobin-C Diseases

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Hemoglobin C Disease

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemoglobinopathies
Hemoglobin C Disease

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Hemoglobin C Disease

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Hemoglobin C Disease