Anemia, Hemolytic, Congenital Nonspherocytic

MeSH 搜索器

Anemia, Hemolytic, Congenital Nonspherocytic

Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

推出的年份: 1991(8268)

树号: C15.378.071.141.150.100, C16.320.070.100

MeSH 单一 ID: D000746

进入的组:

Anemia, Hemolytic Congenital, Nonspherocytic
Hemolytic Anemia, Congenital Nonspherocytic
Anemia, Congenital Nonspherocytic Hemolytic
Congenital Nonspherocytic Hemolytic Anemia

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]
        
        Anemia, Dyserythropoietic, Congenital [C15.378.071.141.150.095]
        
        Anemia, Hemolytic, Congenital Nonspherocytic [C15.378.071.141.150.100]
        
        Anemia, Sickle Cell [C15.378.071.141.150.150] add_circle
        
        Elliptocytosis, Hereditary [C15.378.071.141.150.365]
        
        Glucosephosphate Dehydrogenase Deficiency [C15.378.071.141.150.480] add_circle
        
        Hemoglobin C Disease [C15.378.071.141.150.490]
        
        Spherocytosis, Hereditary [C15.378.071.141.150.785]
        
        Thalassemia [C15.378.071.141.150.875] add_circle

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Anemia, Hemolytic, Congenital [C16.320.070]

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MeSH 搜索器

Anemia, Hemolytic, Congenital Nonspherocytic

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