Informaţii despre

Nume Prothrombin Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificare anatomică Malacards Blood diseases

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Boli A-Z Acanthamoeba Keratitis Acquired Hemophilia Acquired Hemophilia a Acquired Hypoprothrombinemia Acquired Von Willebrand Syndrome Acute Liver Failure Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Analbuminemia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Breast Reconstruction Budd-Chiari Syndrome Buerger Disease Cardiac Tamponade Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Cerebritis Compartment Syndrome Congenital Disorder of Glycosylation, Type Ia Coronary Thrombosis Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Eclampsia Endocarditis Esophageal Varix Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Follicular Lymphoma Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Homocysteinemia Homocystinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypersplenism Immune System Disease Inherited Blood Coagulation Disease Inherited Hypoprothrombinemia Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Kindler Syndrome Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Liver Disease Lymphoma Marantic Endocarditis May-Thurner Syndrome Meningococcemia Mesenteric Vascular Occlusion Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Osteonecrosis Papilledema Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency, Congenital Pulmonary Alveolar Microlithiasis Pulmonary Embolism Purpura Purpura Fulminans Pyoderma Qualitative Platelet Defect Raynaud Disease Renal Glucosuria Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Scabies Scott Syndrome Severe Hemophilia a Severe Hemophilia B Severe Pre-Eclampsia Shwartzman Phenomenon Sjogren Syndrome Sneddon Syndrome Spinal Cord Infarction Splenic Disease Splenic Infarction Spotted Fever Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Varicose Veins Vasculitis Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2