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© May 2005 Lorentz JÄNTSCHI && Sorana Daniela BOLBOACĂ

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 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