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Prevalence Statistics for Types of Bleeding and coagulation conditions

Prevalence Statistics for Types of Bleeding and coagulation conditions

The information below shows a list of types of Bleeding and coagulation conditions, with information as to the prevalence of each of these types. Estimates of the people affected are calculated based on the available statistic.

Disease Prevalence Estimate US people estimate Statistic Used for Calculation
Enterohemorrhagic E. Coli infection N/A N/A No information
Embolism N/A N/A No information
Pulmonary embolism N/A N/A No information
Thromboembolism N/A N/A No information
Subconjunctival hemorrhage N/A N/A No information
Gastrointestinal bleeding N/A N/A No information
Stomach bleeding N/A N/A No information
Intestinal bleeding N/A N/A No information
Rectal bleeding N/A N/A No information
Black eye N/A N/A No information
Von Willebrand disease, type 3 N/A N/A No information
Von Willebrand disease, type 2N N/A N/A No information
Von Willebrand disease, type 2M N/A N/A No information
Von Willebrand disease, type 2B N/A N/A No information
Von Willebrand disease, type 2A N/A N/A No information
Von Willebrand disease, type 2 N/A N/A No information
Von Willebrand disease, type 1 N/A N/A No information
Decreased protein C N/A N/A No information
Decreased protein S N/A N/A No information
Factor X deficiency N/A N/A No information
Factor X deficiency -- San Antonio N/A N/A No information
Factor X deficiency -- Friuli N/A N/A No information
Factor X deficiency -- Padua N/A N/A No information
Factor X deficiency -- Nottingham N/A N/A No information
Factor X deficiency -- Kanazawa N/A N/A No information
Factor X deficiency -- Shanghai N/A N/A No information
Factor X deficiency -- St. Louis II N/A N/A No information
Factor X deficiency -- Stockton N/A N/A No information
Factor X deficiency -- Taunton N/A N/A No information
Factor X deficiency -- Vorarlberg N/A N/A No information
Factor X deficiency -- Wenatchee I N/A N/A No information
Factor X deficiency -- Wenatchee II N/A N/A No information
Factor X deficiency -- Santo Domingo N/A N/A No information
Factor X deficiency -- Ketchikan N/A N/A No information
Factor X deficiency -- Tokyo N/A N/A No information
Factor X deficiency -- autosomal dominant N/A N/A No information
Hemorrhagic prostatic cyst N/A N/A No information
Posthemorrhagic anemia N/A N/A No information
Immune Thrombocytopenic Purpura N/A N/A rare.
Autoimmune Thrombocytopenia N/A N/A No information
Autoimmune Hemophilia N/A N/A No information
Factor VII deficiency N/A N/A No information
Shock, Hemorrhagic N/A N/A No information
Venous Thrombosis N/A N/A No information
Variceal Bleeding N/A N/A No information
Intracranial Hemorrhages N/A N/A No information
Intracranial Embolism N/A N/A No information
Chronic liver disease like bleeding tendencies N/A N/A No information
Colitis like hematochezia N/A N/A No information
Intraocular hemorrhage N/A N/A No information
Glomerulonephritis-like microscopic hematuria N/A N/A No information
ITP-like ecchymoses N/A N/A No information
Periodontitis-like bleeding gums N/A N/A No information
Postoperative Hemorrhage N/A N/A No information
Cerebral hemorrhage N/A N/A No information
Rift Valley Fever N/A N/A No information
Viral Hemorrhagic Fevers N/A N/A No information
Subarachnoid haemorrhage N/A N/A No information
Hemorrhage N/A N/A No information
Postpartum hemorrhage N/A N/A No information
Hemoptysis N/A N/A No information
Hematemesis N/A N/A No information
Osler's disease N/A N/A No information
Hemothorax N/A N/A No information
Thrombosis N/A N/A No information
Purpura N/A N/A No information
Deep vein thrombosis N/A N/A No information
Hematuria N/A N/A No information
Transient bleeding N/A N/A No information
Mild bleeding N/A N/A No information
Caterpillar-induced bleeding syndrome N/A N/A No information
Caterpillar-induced bleeding syndrome -- Lonomia achelous N/A N/A No information
Caterpillar-induced bleeding syndrome -- Lonomia obliqua N/A N/A No information
Acquired amegakaryocytic thrombocytopenia N/A N/A No information
Clotting disorders N/A N/A No information
Bleeding disorders N/A N/A No information
Hemophilia approx 1 in 13,600 or 0.01% or 20,000 people in USA 20,000 20,000 people in the United States (NHLBI)
Christmas disease N/A N/A No information
Von Willebrand disease approx 1 in 90 or 1.10% or 3 million people in USA 2,999,999 estimated 3 million mostly undiagnosed
Hemophilia A N/A N/A No information
Hemophilia B N/A N/A No information
The Hemophilias N/A N/A No information
Hemophilic arthropathy N/A N/A No information
Nosebleeds N/A N/A No information
Factor XIII deficiency, congenital N/A N/A No information
Factor XIII Deficiency N/A N/A No information
Factor XIII, A1 subunit Deficiency N/A N/A No information
Factor XIII, B subunit Deficiency N/A N/A No information
Factor V and factor VIII, combined deficiency of N/A N/A No information
Hageman factor deficiency N/A N/A No information
Stuart factor deficiency, acquired N/A N/A No information
Stuart factor deficiency, congenital N/A N/A No information
Factor V deficiency N/A N/A No information
Factor 8 deficiency, congenital N/A N/A No information
Factor XI deficiency, congenital N/A N/A No information
Factor V Quebec N/A N/A No information
Factor XII Deficiency N/A N/A No information
Factor IX Deficiency N/A N/A No information
Factor V Leiden mutation N/A N/A No information
ATRUS syndrome N/A N/A No information
Portal vein thrombosis N/A N/A No information
Vitamin K deficiency N/A N/A No information
Hemospermia N/A N/A No information
Coagulopathy N/A N/A No information
Anticoagulant poisoning N/A N/A No information
Neurofibromatosis-Noonan syndrome N/A N/A No information
Portal thrombosis N/A N/A No information
Alba/Geneva I dysfibrinogenemia N/A N/A No information
Adelaide I dysfibrinogenemia N/A N/A No information
Troyes dysfibrinogenemia N/A N/A No information
Saint Louis dysfibrinogenemia N/A N/A No information
Zurich II dysfibrinogenemia N/A N/A No information
Metz dysfibrinogenemia N/A N/A No information
Oslo dysfibrinogenemia N/A N/A No information
Leuven dysfibrinogenemia N/A N/A No information
Vancouver dysfibrinogenemia N/A N/A No information
Bethesda II dysfibrinogenemia N/A N/A No information
Dysfibrinogenemia, familial N/A N/A No information
Asahi I dysfibrinogenemia N/A N/A No information
Oklahoma dysfibrinogenemia N/A N/A No information
Aarhus dysfibrinogenemia N/A N/A No information
Nancy dysfibrinogenemia N/A N/A No information
Baltimore dysfibrinogenemia N/A N/A No information
Paris II dysfibrinogenemia N/A N/A No information
Detroit dysfibrinogenemia N/A N/A No information
Zurich I dysfibrinogenemia N/A N/A No information
Los Angeles dysfibrinogenemia N/A N/A No information
Paris I dysfibrinogenemia N/A N/A No information
Aarau dysfibrinogenemia N/A N/A No information
Bethesda I dysfibrinogenemia N/A N/A No information
Cleveland dysfibrinogenemia N/A N/A No information
Almeria I dysfibrinogenemia N/A N/A No information
Wiesbaden dysfibrinogenemia N/A N/A No information
Parma dysfibrinogenemia N/A N/A No information
Amiens I dysfibrinogenemia N/A N/A No information
Ales dysfibrinogenemia N/A N/A No information
Amsterdam dysfibrinogenemia N/A N/A No information
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type N/A N/A No information
Hemorrhagic proctocolitis N/A N/A No information
Hemorrhagic thrombocythemia N/A N/A No information
Essential thrombocytopenia N/A N/A No information
Essential thrombocytosis -- same as essential thrombocythemia N/A N/A No information
Hereditary thrombocythemia N/A N/A No information
Argentinean hemorrhagic fever N/A N/A No information
Bolivian hemorrhagic fever N/A N/A No information
Acquired prothrombin complex deficiency N/A N/A No information
Ebola N/A N/A No information
Dengue fever N/A N/A No information
Yellow fever N/A N/A No information
Lassa fever N/A N/A No information
Marburg virus N/A N/A No information
Dengue hemorrhagic fever N/A N/A No information
Antiphospholipid syndrome N/A N/A No information
Vocal cord hemorrhage N/A N/A No information
Postoperative haemorrhage N/A N/A No information
Postpartum haemorrhage N/A N/A No information
Osler-Rendu-Weber syndrome 2 N/A N/A No information
Osler-Rendu-Weber syndrome 3 N/A N/A No information
Protein S acquired deficiency N/A N/A No information
Angiodysplasia N/A N/A No information
Hypofibrinogenemia, congenital N/A N/A No information
Hereditary macrothrombocytopenia N/A N/A No information
Congenital amegakaryocytic thrombocytopenia N/A N/A No information
Capillary leak syndrome with monoclonal gammopathy N/A N/A No information
Prekallikrein deficiency, congenital N/A N/A No information
Protein C deficiency N/A N/A No information
Congenital thrombotic disease due to protein C deficiency N/A N/A No information
Homozygous protein C deficiency N/A N/A No information
Protein S deficiency N/A N/A No information
Hemoglobin E disease N/A N/A No information
Macrothrombocytopenia -- progressive deafness N/A N/A No information
Omsk hemorrhagic fever N/A N/A No information
Hemorragic fever with renal syndrome N/A N/A No information
Hemorrhagic fever N/A N/A No information
Hyphema N/A N/A No information
Kyasanur-Forrest disease N/A N/A No information
Antithrombin Deficiency, type I N/A N/A No information
Antithrombin Deficiency, type II N/A N/A No information
Antithrombin Deficiency N/A N/A No information
Antithrombin III deficiency, congenital N/A N/A No information
Acquired prothrombin deficiency N/A N/A No information
Acquired hypoprothrombinemia N/A N/A No information
Prothrombin deficiency N/A N/A No information
Congenital Antithrombin III Deficiency N/A N/A No information
Glanzmann Thrombasthenia N/A N/A No information
Defibrination syndrome N/A N/A No information
Fibrinogen deficiency, congenital N/A N/A No information
Familial primary cryofibrinogenemia N/A N/A No information
Cryofibrinogenemia N/A N/A No information
Hypofibrinogenemia, familial N/A N/A No information
Congenital Afibrinogenemia N/A N/A No information
Von Willebrand disease, recessive form N/A N/A No information
Willebrand disease, acquired N/A N/A No information
Von Willebrand disease, dominant form N/A N/A No information
Thrombocytopenia N/A N/A No information
X-linked dyserythropoietic anaemia and thrombocytopenia N/A N/A No information
Thrombotic thrombocytopenic purpura, congenital N/A N/A No information
Purpura simplex N/A N/A No information
Senile purpura N/A N/A No information
Thrombotic thrombocytopenic purpura, acquired approx 1 in 68 or 1.47% or 4 million people in USA 3,999,999 estimated 4-7 million people are diagnosed with thrombotic thrombocytopenic purpura each year in the US, Genetics Home Reference website
Thrombasthenia N/A N/A No information
Thrombocytopenic purpura, autoimmune N/A N/A No information
Henoch-Schonlein purpura N/A N/A No information
Purpura simplex, sporadic N/A N/A No information
Purpura simplex, hereditary N/A N/A No information
Pulmonary haemosiderosis, primary N/A N/A No information
Idiopathic pulmonary hemosiderosis N/A N/A No information
Hemosiderosis N/A N/A No information
Superficial siderosis of the central nervous system N/A N/A No information
Epstein's Syndrome N/A N/A No information
Thrombocytopenia -- Multiple Congenital Anomalies N/A N/A No information
Alport syndrome with macrothrombocytopenia N/A N/A No information
Alport Syndrome approx 1 in 50,000 or 0.00% or 5,440 people in USA 5,440 1 per 50,000 newborns suffer from Alport syndrome, Genetics Home Reference website
Amegakaryocytic thrombocytopenia N/A N/A No information
Phocomelia -- thrombocytopenia -- encephalocele -- urogenital malformation N/A N/A No information
Blood coagulation disorders, inherited N/A N/A No information
Acute cholinergic dysautonomia N/A N/A No information
Quebec platelet disorder N/A N/A No information
Thrombocytopenia -- cerebellar hypoplasia -- short stature N/A N/A No information
Von Willebrand disease, platelet type N/A N/A No information
Storage pool platelet disease N/A N/A No information
Storage pool platelet deficiency, SPD N/A N/A No information
Gray platelet syndrome N/A N/A No information
Tidal platelet dysgenesis N/A N/A No information
Thrombocytopathy N/A N/A No information
Catastrophic Antiphospholipid Syndrome N/A N/A No information
Fetal and neonatal alloimmune thrombocytopenia N/A N/A No information
Heparin-induced thrombocytopenia N/A N/A No information
Multiple sclerosis -- ichthyosis -- factor 8 deficiency N/A N/A No information
Thrombocytopenia -- chromosome breakage N/A N/A No information
Thrombocytopathy -- asplenia -- miosis N/A N/A No information
Thrombocytopenia X-linked N/A N/A No information
Thrombocytopenia -- Robin sequence N/A N/A No information
Adrenal hemorrhage, neonatal N/A N/A No information
Hemorrhagic shock and encephalopathy syndrome N/A N/A No information
Fochs-LADD N/A N/A No information
Hypercoagulability syndrome, due to glycosylphosphatidylinositol deficiency N/A N/A No information
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency N/A N/A No information
Aantibodies anti-FVIIIc syndrome N/A N/A No information
Hemangioma thrombocytopenia syndrome N/A N/A No information
Altamira syndrome N/A N/A No information
Buerger's disease N/A N/A No information
DIC N/A N/A No information
Hermansky-Pudlak Syndrome N/A N/A No information
May-Hegglin Anomaly N/A N/A No information
Bernard-Soulier Syndrome N/A N/A No information
Thrombocytopenia, cyclic N/A N/A No information
Owren Parahemophilia N/A N/A No information
May-Hegglin thrombocytopenia N/A N/A No information
Fibronectin-Deficient EDS N/A N/A No information
Korovnikov syndrome N/A N/A No information
Portsmouth syndrome N/A N/A No information
Immune thrombocytopenia N/A N/A No information
Anti-plasmin deficiency, congenital N/A N/A No information
Lemierre's syndrome N/A N/A No information
Shwartzman phenomenon N/A N/A No information
Plasminogen activitor inhibitor type 1 deficiency, congenital N/A N/A No information
Diffuse neonatal hemangiomatosis N/A N/A No information
Paris-Trousseau thrombocytopenia N/A N/A No information
Plasminogen deficiency, congenital N/A N/A No information
Thrombomodulin anomalies, familial N/A N/A No information
Schlegelberger-Grote syndrome N/A N/A No information
Fitzgerald-Williams-Flaujeac trait N/A N/A No information
Epstein (C.J.) syndrome N/A N/A No information
Evan's syndrome N/A N/A No information
Waterhouse-Friederichsen syndrome N/A N/A No information
Hereditary hemorrhagic telangiectasia approx 1 in 5,000 or 0.02% or 54,400 people in USA 54,399 estimated 1 per 5,000 - 10,000 people suffer from hereditary hemorrhagic telangiectasia worldwide, Genetics Home Reference website
TAR syndrome N/A N/A No information
Hermansky-Pudlak syndrome type 2 N/A N/A No information

Types of Bleeding and coagulation conditions

For more information about types of Bleeding and coagulation conditions, refer to our section on types of Bleeding and coagulation conditions.

About prevalence:

The medical term 'prevalence' of Bleeding and coagulation conditions usually refers to the estimated population of people who are managing Bleeding and coagulation conditions at any given time, whereas the annual diagnosis rate of new cases of Bleeding and coagulation conditions is called the 'incidence'. For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.

 

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