This section presents information about the death rate statistics
for the various types of Bleeding and coagulation conditions.
Disease | Death Rate Estimate | US deaths estimate | Statistic Used for Calculation |
| Enterohemorrhagic E. Coli infection |
N/A |
N/A |
No information
|
| Embolism |
N/A |
N/A |
No information
|
| Pulmonary embolism |
unavailable |
|
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 |
unavailable |
|
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 people in the United States (NHLBI) |
20,000 people in the United States (NHLBI)
|
| Christmas disease |
N/A |
N/A |
No information
|
| Von Willebrand disease |
N/A |
N/A |
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 |
N/A |
N/A |
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 |
N/A |
N/A |
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 |
N/A |
N/A |
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
|
