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2008 MeSH

MeSH Descriptor Data

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Hemostatic Disorders
MeSH HeadingHemostatic Disorders
Tree NumberC14.907.454
Tree NumberC15.378.463.835
Scope NotePathological processes involving the integrity of blood circulation. Hemostasis depends on the integrity of BLOOD VESSELS, blood fluidity, and BLOOD COAGULATION. Majority of the hemostatic disorders are caused by disruption of the normal interaction between the VASCULAR ENDOTHELIUM, the plasma proteins (including BLOOD COAGULATION FACTORS), and PLATELETS.
Entry TermHemostatic Disorders, Vascular
Entry TermVascular Hemostatic Disorders
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
History Note2008 (1999)
Date of Entry19980611
Unique IDD020141


MeSH Tree Structures

 
Cardiovascular Diseases [C14]
   Vascular Diseases [C14.907]
Aneurysm [C14.907.055]  +
Angiodysplasia [C14.907.075]  +
Angiomatosis [C14.907.077]  +
Angioedema [C14.907.079]  +
Aortic Diseases [C14.907.109]  +
Arterial Occlusive Diseases [C14.907.137]  +
Arteriovenous Malformations [C14.907.150]  +
Arteritis [C14.907.184]  +
Capillary Leak Syndrome [C14.907.218]
Cerebrovascular Disorders [C14.907.253]  +
Colitis, Ischemic [C14.907.286]
Compartment Syndromes [C14.907.303]  +
Diabetic Angiopathies [C14.907.320]  +
Embolism and Thrombosis [C14.907.355]  +
Hand-Arm Vibration Syndrome [C14.907.440]
Hemorrhoids [C14.907.449]
Hemostatic Disorders [C14.907.454]
Cryoglobulinemia [C14.907.454.140]
Ehlers-Danlos Syndrome [C14.907.454.240]
Hemangioma, Cavernous [C14.907.454.385]  +
Multiple Myeloma [C14.907.454.460]
Pseudoxanthoma Elasticum [C14.907.454.530]
Purpura, Hyperglobulinemic [C14.907.454.550]
Scurvy [C14.907.454.800]
Shwartzman Phenomenon [C14.907.454.810]
Telangiectasia, Hereditary Hemorrhagic [C14.907.454.900]
Waldenstrom Macroglobulinemia [C14.907.454.960]
Hepatic Veno-Occlusive Disease [C14.907.460]
Hyperemia [C14.907.474]
Hypertension [C14.907.489]  +
Hypotension [C14.907.514]  +
Myocardial Ischemia [C14.907.585]  +
Optic Neuropathy, Ischemic [C14.907.601]
Peripheral Vascular Diseases [C14.907.617]  +
Pulmonary Veno-Occlusive Disease [C14.907.690]
Reperfusion Injury [C14.907.725]  +
Retinal Vein Occlusion [C14.907.760]
Scimitar Syndrome [C14.907.780]
Spinal Cord Vascular Diseases [C14.907.790]  +
Splenic Infarction [C14.907.795]
Superior Vena Cava Syndrome [C14.907.800]
Telangiectasis [C14.907.823]  +
Thoracic Outlet Syndrome [C14.907.863]  +
Varicocele [C14.907.903]
Varicose Veins [C14.907.927]  +
Vascular Fistula [C14.907.933]  +
Vascular Neoplasms [C14.907.936]
Vasculitis [C14.907.940]  +
Venous Insufficiency [C14.907.952]  +

 
Hemic and Lymphatic Diseases [C15]
   Hematologic Diseases [C15.378]
      Hemorrhagic Disorders [C15.378.463]
Afibrinogenemia [C15.378.463.067]
Bernard-Soulier Syndrome [C15.378.463.080]
Disseminated Intravascular Coagulation [C15.378.463.250]
Factor V Deficiency [C15.378.463.300]
Factor VII Deficiency [C15.378.463.310]
Factor X Deficiency [C15.378.463.320]
Factor XI Deficiency [C15.378.463.325]
Factor XII Deficiency [C15.378.463.330]
Factor XIII Deficiency [C15.378.463.335]
Hemophilia A [C15.378.463.500]
Hemophilia B [C15.378.463.510]
Hypoprothrombinemias [C15.378.463.550]
Platelet Storage Pool Deficiency [C15.378.463.735]  +
Purpura, Thrombocytopenic, Idiopathic [C15.378.463.740]
Thrombasthenia [C15.378.463.810]
Thrombocythemia, Hemorrhagic [C15.378.463.825]
Hemostatic Disorders [C15.378.463.835]
Cryoglobulinemia [C15.378.463.835.140]
Ehlers-Danlos Syndrome [C15.378.463.835.240]
Hemangioma, Cavernous [C15.378.463.835.385]  +
Multiple Myeloma [C15.378.463.835.460]
Pseudoxanthoma Elasticum [C15.378.463.835.530]
Purpura, Hyperglobulinemic [C15.378.463.835.550]
Purpura, Schoenlein-Henoch [C15.378.463.835.580]
Scurvy [C15.378.463.835.800]
Shwartzman Phenomenon [C15.378.463.835.810]
Telangiectasia, Hereditary Hemorrhagic [C15.378.463.835.900]
Waldenstrom Macroglobulinemia [C15.378.463.835.960]
Vitamin K Deficiency [C15.378.463.841]  +
von Willebrand Disease [C15.378.463.920]
Waterhouse-Friderichsen Syndrome [C15.378.463.950]
Wiskott-Aldrich Syndrome [C15.378.463.960]

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