Informaţii despre

Nume Acquired Hemophilia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Acquired coagulation factor deficiency
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Acquired Hemophilia a; Hemophilia a; Hemophilia B; Severe Hemophilia a; Severe Hemophilia B

Vezi şi

Boli A-Z Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Pancreatitis Afibrinogenemia Afibrinogenemia, Congenital Aging Alcohol-Related Birth Defect Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Anca-Associated Vasculitis Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Autoimmune Disease Autoimmune Pancreatitis Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Platelet Disease Budd-Chiari Syndrome Bullous Pemphigoid Cardiac Tamponade Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Cholecystitis Chorioamnionitis Chronic Neutrophilic Leukemia Colitis Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Diabetes Mellitus Disseminated Intravascular Coagulation Duodenitis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Esophageal Cancer Essential Thrombocythemia 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 Fournier Gangrene Gastric Cancer Gastrointestinal Stromal Tumor Glanzmann Thrombasthenia Hemarthrosis Hematopoietic Stem Cell Transplantation Hemolytic Anemia Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatitis Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hypereosinophilic Syndrome Inherited Blood Coagulation Disease Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Leech Infestation Lemierre's Syndrome Leukemia Lung Cancer Lung Disease Lupus Erythematosus Lymphoma Mild Hemophilia a Multicentric Castleman Disease Multiple Sclerosis Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myeloproliferative Neoplasm Pancreatitis Pemphigus Pemphigus Foliaceus Pemphigus Vulgaris Pericardial Effusion Peripheral Vertigo Placenta Disease Pneumonia Post-Thrombotic Syndrome Prostate Cancer Prostatitis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Embolism Purpura Pustular Psoriasis Quebec Platelet Disorder Retinal Artery Occlusion Rheumatoid Arthritis Sagittal Sinus Thrombosis Scott Syndrome Severe Hemophilia a Severe Hemophilia B Skin Disease Stroke, Ischemic Systemic Lupus Erythematosus Thrombasthenia Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Vasculitis Vein Disease Von Willebrand's Disease Von Willebrand Disease, Type 1