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delta-Thalassemia

A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of HEMOGLOBIN A2, a minor component of adult hemoglobin monitored in the diagnosis of BETA-THALASSEMIA.

Year introduced: 2009

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Subheadings:

Tree Number(s): C15.378.050.141.150.875.575, C15.378.420.826.200, C16.320.070.875.575, C16.320.365.826.575

MeSH Unique ID: D055538

Entry Terms:

  • delta Thalassemia
  • delta-Thalassemias

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