Hemoglobin C Disease

MeSH 搜索器

Hemoglobin C Disease

A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.

推出的年份: 1972(1966)

树号: C15.378.071.141.150.490, C15.378.420.463, C16.320.070.490, C16.320.365.463

MeSH 单一 ID: D006445

进入的组:

C Disease, Hemoglobin
C Diseases, Hemoglobin
Hemoglobin C Diseases
Hemoglobin-C Disease
Hemoglobin-C Diseases

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
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Hemoglobinopathies [C15.378.420]

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

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Hemoglobinopathies [C16.320.365]

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Hemoglobin C Disease

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