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Hemorrhagic Disorders

More information in Books or onNLM PubMed
Definition: Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS).  "predisposition to abnormal hemostasis"; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES   
See Also Hemostatic Disorders
Examples Afibrinogenemia; Bernard-Soulier Syndrome; Disseminated Intravascular Coagulation; Factor V Deficiency; Factor VII Deficiency; Factor X Deficiency; Factor XI Deficiency; Factor XII Deficiency; Factor XIII Deficiency; Hemophilia A; Hemophilia B; Hemostatic Disorders; Hypoprothrombinemias; Platelet Storage Pool Deficiency; Purpura, Thrombocytopenic, Idiopathic; Thrombasthenia; Thrombocythemia, Essential; Vitamin K Deficiency; von Willebrand Diseases; Waterhouse-Friderichsen Syndrome; Wiskott-Aldrich Syndrome 		Other names Hemorrhagic Disorder; Hemorrhagic Diatheses; Disorders, Hemorrhagic; Disorder, Hemorrhagic; Diathesis, Hemorrhagic; Diatheses, Hemorrhagic; Hemorrhagic Diathesis
 
SubstanceCAS Registry & nameCategoriesSource
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells  0   *Albinism *Hemorrhagic Disorders *Hermanski-Pudlak Syndrome.
Alpha-2-plasmin inhibitor deficiency  0   *Hemorrhagic Disorders alpha-2-Antiplasmin/deficiency.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
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