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 C15 Hemic and Lymphatic Diseases D006425 +
  C15.378 Hematologic Diseases D006402 +
   C15.378.100 Blood Coagulation Disorders D001778 +
    C15.378.100.425 Blood Coagulation Disorders, Inherited D025861 +
      C15.378.100.425.056 Afibrinogenemia D000347 
      C15.378.100.425.080 Bernard-Soulier Syndrome D001606 
      C15.378.100.425.510 Hemophilia B D002836 
      C15.378.100.425.300 Factor V Deficiency D005166 
      C15.378.100.425.310 Factor VII Deficiency D005168 
      C15.378.100.425.320 Factor X Deficiency D005171 
      C15.378.100.425.325 Factor XI Deficiency D005173 
      C15.378.100.425.330 Factor XII Deficiency D005175 
      C15.378.100.425.335 Factor XIII Deficiency D005177 
      C15.378.100.425.500 Hemophilia A D006467 
      C15.378.100.425.550 Hypoprothrombinemias D007020 
      C15.378.100.425.820 Thrombasthenia D013915 
      C15.378.100.425.900 von Willebrand Disease D014842 
      C15.378.100.425.970 Wiskott-Aldrich Syndrome D014923 
      C15.378.100.425.037 Activated Protein C Resistance D020016 
      C15.378.100.425.690 Protein C Deficiency D020151 
      C15.378.100.425.075 Antithrombin III Deficiency D020152 
      C15.378.100.425.515 Hermanski-Pudlak Syndrome D022861 
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.099 Blood Coagulation Disorders, Inherited D025861 +
     C16.320.099.056 Afibrinogenemia D000347 
     C16.320.099.080 Bernard-Soulier Syndrome D001606 
     C16.320.099.510 Hemophilia B D002836 
     C16.320.099.300 Factor V Deficiency D005166 
     C16.320.099.310 Factor VII Deficiency D005168 
     C16.320.099.320 Factor X Deficiency D005171 
     C16.320.099.325 Factor XI Deficiency D005173 
     C16.320.099.330 Factor XII Deficiency D005175 
     C16.320.099.335 Factor XIII Deficiency D005177 
     C16.320.099.500 Hemophilia A D006467 
     C16.320.099.550 Hypoprothrombinemias D007020 
     C16.320.099.820 Thrombasthenia D013915 
     C16.320.099.900 von Willebrand Disease D014842 
     C16.320.099.970 Wiskott-Aldrich Syndrome D014923 
     C16.320.099.037 Activated Protein C Resistance D020016 
     C16.320.099.690 Protein C Deficiency D020151 
     C16.320.099.075 Antithrombin III Deficiency D020152 
     C16.320.099.515 Hermanski-Pudlak Syndrome D022861