Informaţii despre

Nume Afibrinogenemia, Congenital
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary deficiency of other clotting factors
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Cor Pulmonale Acute Myocardial Infarction Acute Pulmonary Heart Disease Afibrinogenemia Aging Aland Island Eye Disease Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Cardiac Tamponade Carotid Artery Thrombosis Cellulitis Central Serous Chorioretinopathy Cerebral Arteritis Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Chronic Thromboembolic Pulmonary Hypertension Cold Urticaria Complement Component 3 Deficiency Complement Factor I Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Constrictive Pericarditis Coronary Thrombosis Corpus Luteum Cyst Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Dysfibrinogenemia, Congenital Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Enterocolitis Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fanconi Anemia, Complementation Group E Fibrinolytic Defect Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemopneumothorax Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Homocysteinemia Immune System Disease Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Liver Disease Marantic Endocarditis Marfan Syndrome Mild Hemophilia a Myocardial Infarction Osteomyelitis Osteonecrosis Patent Foramen Ovale Pericarditis Periodontitis Peripheral Vertigo Peritonitis Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Portal Vein Thrombosis Post-Thrombotic Syndrome Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Retinal Artery Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Severe Hemophilia a Sneddon Syndrome Spinal Cord Infarction Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Varicose Veins Vein Disease Venous Insufficiency Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3