Protein C Deficiency

MeSH 搜索器

Protein C Deficiency

An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.)

推出的年份: 1999

树号: C15.378.100.100.690, C15.378.147.880, C15.378.925.795, C16.320.099.690

MeSH 单一 ID: D020151

进入的组:

Hereditary Thrombophilia Due To Protein C Deficiency
Deficiency, Protein C
Deficiencies, Protein C
Protein C Deficiencies

早前的内容:

Blood Proteins (1981-1987)
Glycoproteins (1981-1987)
Protein C (1987-1998)

All MeSH Categories
- Diseases Category
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Blood Coagulation Disorders [C15.378.100]
        
        Blood Coagulation Disorders, Inherited [C15.378.100.100]
        
        Activated Protein C Resistance [C15.378.100.100.037]
        
        Afibrinogenemia [C15.378.100.100.056]
        
        Antithrombin III Deficiency [C15.378.100.100.075]
        
        Bernard-Soulier Syndrome [C15.378.100.100.080]
        
        Factor V Deficiency [C15.378.100.100.300]
        
        Factor VII Deficiency [C15.378.100.100.310]
        
        Factor X Deficiency [C15.378.100.100.320]
        
        Factor XI Deficiency [C15.378.100.100.325]
        
        Factor XII Deficiency [C15.378.100.100.330]
        
        Factor XIII Deficiency [C15.378.100.100.335]
        
        Hemophilia A [C15.378.100.100.500]
        
        Hemophilia B [C15.378.100.100.510]
        
        Hermanski-Pudlak Syndrome [C15.378.100.100.515]
        
        Hypoprothrombinemias [C15.378.100.100.550]
        
        Protein C Deficiency [C15.378.100.100.690]
        
        Thrombasthenia [C15.378.100.100.820]
        
        von Willebrand Diseases [C15.378.100.100.900] add_circle
        
        Wiskott-Aldrich Syndrome [C15.378.100.100.970]

All MeSH Categories
- Diseases Category
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Blood Protein Disorders [C15.378.147]

All MeSH Categories
- Diseases Category
  - Hemic and Lymphatic Diseases [C15]
    - Hematologic Diseases [C15.378]
      - Thrombophilia [C15.378.925]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Blood Coagulation Disorders, Inherited [C16.320.099]

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MeSH 搜索器

Protein C Deficiency

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