Informaţii despre

Nume Factor Xi Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary factor XI deficiency
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge

Vezi şi

Boli A-Z Acquired Agranulocytosis Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Myocardial Infarction Afibrinogenemia Afibrinogenemia, Congenital Aging Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome 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 Budd-Chiari Syndrome Cardiac Tamponade Carotid Artery Occlusion Cataract Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Cervicitis Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Congenital Disorder of Glycosylation, Type Iic Congenital Ectropion Uveae Conotruncal Heart Malformations Coronary Thrombosis Disseminated Intravascular Coagulation Dysfibrinogenemia Ectropion Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fibrous Histiocytoma Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Glomerulonephritis Hantavirus Pulmonary Syndrome Hemarthrosis Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Histiocytoma Hypersplenism Immune System Disease Inherited Blood Coagulation Disease Intermediate Uveitis Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Juvenile Rheumatoid Arthritis Korean Hemorrhagic Fever Leech Infestation Lissencephaly 1 Listeriosis Lung Cancer Lupus Erythematosus Marantic Endocarditis Membranoproliferative Glomerulonephritis Myocardial Infarction Myositis Myositis Ossificans Nonarteritic Anterior Ischemic Optic Neuropathy Patent Foramen Ovale Peripheral Vertigo Placental Abruption Portal Vein Thrombosis Post-Thrombotic Syndrome Prader-Willi Syndrome Prekallikrein Deficiency Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Rapp-Hodgkin Syndrome Retinal Artery Occlusion Retinitis Rheumatoid Arthritis Sagittal Sinus Thrombosis Severe Hemophilia a Severe Hemophilia B Sneddon Syndrome Spinal Cord Infarction Splenic Disease Squamous Cell Carcinoma Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Tetraamelia Syndrome, Autosomal Recessive Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thymoma Thyroiditis Vein Disease Ventricular Fibrillation, Paroxysmal Familial, 1 Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1