Disease Browser
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Parent Node: Hemorrhagic Disorders (D006474) |
..Starting node ..Antithrombin, Familial Hemorrhagic Diathesis due to (C565947)
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Child Nodes:
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Sister Nodes: |
..Afibrinogenemia (D000347) 3
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..Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells (C538539)
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..Anti-plasmin deficiency, congenital (C537777)
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..Antithrombin, Familial Hemorrhagic Diathesis due to (C565947)
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..Bernard-Soulier Syndrome (D001606) 5
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..Disseminated Intravascular Coagulation (D004211)
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..Factor V Deficiency (D005166) 4
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..Factor VII Deficiency (D005168)
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..Factor X Deficiency (D005171)
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..Factor XI Deficiency (D005173)
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..Factor XII Deficiency (D005175)
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..Factor XIII Deficiency (D005177) 2
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..Hemophilia A (D006467) 5
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..Hemophilia B (D002836)
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..HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730)
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..Hemostatic Disorders (D020141) 48
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..Hypoprothrombinemias (D007020) 2
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..Plasminogen Activator Inhibitor-1 Deficiency (C567640)
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..Platelet Storage Pool Deficiency (D010981) 5
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..Purpura, Thrombocytopenic, Idiopathic (D016553)
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..Thrombasthenia (D013915) 3
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..Thrombocythemia, Essential (D013920)
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..Vitamin K Deficiency (D014813) 1
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..von Willebrand Diseases (D014842) 6
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..Waterhouse-Friderichsen Syndrome (D014884) 1
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..Wiskott-Aldrich Syndrome (D014923) 1
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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