alpha-Thalassemia
A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
Year introduced: 1993
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Subheadings:
Tree Number(s): C15.378.050.141.150.875.100, C15.378.420.826.100, C16.320.070.875.100, C16.320.365.826.100
MeSH Unique ID: D017085
Entry Terms:
- alpha-Thalassemias
- Thalassemia-alpha
- Thalassemia alpha
- Hemoglobin H Disease
- Disease, Hemoglobin H
- Alpha Thalassemia
- Thalassemia, Alpha
- A-Thalassemia
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