alpha-Thalassemia
Also known asalpha-Thalassemias · Thalassemia-alpha · Thalassemia alpha · Hemoglobin H Disease · Disease, Hemoglobin H · Alpha Thalassemia · Thalassemia, Alpha · A-Thalassemia
Definition
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.
MeSH classification
- C15.378.050.141.150.875.100
- C15.378.420.826.100
- C16.320.070.875.100
- C16.320.365.826.100
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Source: NIH MeSH 2026 (D017085) — National Library of Medicine, public domain. View official MeSH record ↗