beta-Thalassemia
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
推出的年份: 1993
树号: C15.378.071.141.150.875.150, C15.378.420.826.150, C16.320.070.875.150, C16.320.365.826.150
MeSH 单一 ID: D017086
进入的组:
Microcytemia, beta Type
Microcytemias, beta Type
Type Microcytemia, beta
Type Microcytemias, beta
beta Type Microcytemia
beta Type Microcytemias
beta Thalassemia
Thalassemia, beta
Thalassemias, beta
beta Thalassemias
Thalassemia, beta Type
Thalassemias, beta Type
Type Thalassemia, beta
Type Thalassemias, beta
beta Type Thalassemia
beta Type Thalassemias
Thalassemia Intermedia
Intermedia, Thalassemia
Intermedias, Thalassemia
Thalassemia Intermedias
Thalassemia Minor
Thalassemia Minor (beta-Thalassemia Minor)
Minor, Thalassemia (beta-Thalassemia Minor)
Minors, Thalassemia (beta-Thalassemia Minor)
Thalassemia Minor (beta Thalassemia Minor)
Thalassemia Minors (beta-Thalassemia Minor)
Hemoglobin F Disease
Disease, Hemoglobin F
Thalassemia Major
Anemia, Erythroblastic
Anemias, Erythroblastic
Erythroblastic Anemia
Thalassemia Major (beta-Thalassemia Major)
Major, Thalassemia (beta-Thalassemia Major)
Majors, Thalassemia (beta-Thalassemia Major)
Thalassemia Major (beta Thalassemia Major)
Thalassemia Majors (beta-Thalassemia Major)
Mediterranean Anemia
Anemias, Mediterranean
Mediterranean Anemias
Anemia, Cooley's
Anemia, Cooley
Anemia, Cooleys
Cooley's Anemia
Anemia, Mediterranean
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