alpha-Thalassemia

MeSH 搜索器

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.

推出的年份: 1993

树号: C15.378.071.141.150.875.100, C15.378.420.826.100, C16.320.070.875.100, C16.320.365.826.100

MeSH 单一 ID: D017085

进入的组:

alpha-Thalassemias
Alpha Thalassemia
Thalassemia, Alpha
Thalassemia-alpha
Thalassemia alpha
A-Thalassemia
Hemoglobin H Disease
Disease, Hemoglobin H

早前的内容:

Thalassemia (1966-1992)

All MeSH Categories
- Diseases Category
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Anemia [C15.378.071]
        
        Anemia, Hemolytic [C15.378.071.141]
        
        Anemia, Hemolytic, Congenital [C15.378.071.141.150]
        
        Thalassemia [C15.378.071.141.150.875]
        
        alpha-Thalassemia [C15.378.071.141.150.875.100]
        
        beta-Thalassemia [C15.378.071.141.150.875.150]
        
        delta-Thalassemia [C15.378.071.141.150.875.575]

All MeSH Categories
- Diseases Category
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Hemoglobinopathies [C15.378.420]
        
        Thalassemia [C15.378.420.826]
        
        alpha-Thalassemia [C15.378.420.826.100]
        
        Hydrops Fetalis [C15.378.420.826.100.350]
        
        beta-Thalassemia [C15.378.420.826.150]
        
        delta-Thalassemia [C15.378.420.826.200]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Anemia, Hemolytic, Congenital [C16.320.070]
        
        Thalassemia [C16.320.070.875]
        
        alpha-Thalassemia [C16.320.070.875.100]
        
        beta-Thalassemia [C16.320.070.875.150]
        
        delta-Thalassemia [C16.320.070.875.575]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Hemoglobinopathies [C16.320.365]
        
        Thalassemia [C16.320.365.826]
        
        alpha-Thalassemia [C16.320.365.826.100]
        
        Hydrops Fetalis [C16.320.365.826.100.350]
        
        beta-Thalassemia [C16.320.365.826.150]
        
        delta-Thalassemia [C16.320.365.826.575]

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