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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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

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Thalassemia
delta-Thalassemia

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemoglobinopathies
Thalassemia
delta-Thalassemia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Thalassemia
delta-Thalassemia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Thalassemia
delta-Thalassemia