Informaţii despre

Nume Afibrinogenemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Afibrinogenemia, Congenital

Vezi şi

Boli A-Z Acquired Angioedema Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Liver Failure Afibrinogenemia, Congenital Aland Island Eye Disease Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Arthus Reaction Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Budd-Chiari Syndrome C3 Glomerulopathy Cardiac Tamponade Carotid Artery Thrombosis Cellulitis Central Retinal Vein Occlusion Cerebral Arteritis Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Chronic Thromboembolic Pulmonary Hypertension Complement Component 3 Deficiency Complement Deficiency Complement Factor H Deficiency Complement Factor I Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Constrictive Pericarditis Coronary Thrombosis Corpus Luteum Cyst Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Dysfibrinogenemia, Congenital Enterocolitis 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 Fainting Fanconi Anemia, Complementation Group E Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Glomerulonephritis Hantavirus Pulmonary Syndrome Head Injury Hellp Syndrome Hemangioma Hemarthrosis Hemoglobin E Disease Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemopneumothorax Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatitis Immune System Disease Inherited Blood Coagulation Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Korean Hemorrhagic Fever Leech Infestation Leiomyoma Lemierre's Syndrome Leukocoria Livedoid Vasculopathy Marfan Syndrome Membranoproliferative Glomerulonephritis Mild Hemophilia a Myocardial Infarction Neisseria Meningitidis Infection Osteomyelitis Paracetamol Poisoning Patent Foramen Ovale Pericarditis Periodontitis Peripheral Vertigo Peritonitis Porencephaly Post-Thrombotic Syndrome Prostatitis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Rapp-Hodgkin Syndrome Retinal Artery Occlusion Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Scott Syndrome Severe Hemophilia a Sneddon Syndrome Spinal Cord Infarction Stroke, Ischemic Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroid Crisis Varicose Veins Variola Minor Vein Disease Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3