Informaţii despre

Nume Von Willebrand's Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Other specified haemorrhagic conditions; Von Willebrand disease
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli cardiovasculare; Boli de sânge

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Liver Failure Acute Myocardial Infarction Afibrinogenemia Afibrinogenemia, Congenital Aging Alcohol-Related Birth Defect Allergic Hypersensitivity Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Angiodysplasia Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Atherosclerosis Arteries, Anomalies of Arteriosclerosis Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia Neuropathy Spectrum Autoimmune Polyglandular Syndrome Type 3 Basal Cell Carcinoma 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 Bombay Phenotype Budd-Chiari Syndrome Cardiac Tamponade Carotid Artery Thrombosis Carpal Tunnel Syndrome Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Arteritis Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Cerebritis Cleft Lip Cleidocranial Dysplasia Coagulation Protein Disease Coats Disease Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Bile Acid Synthesis Defect Congenital Mesoblastic Nephroma Connective Tissue Disease Coronary Thrombosis Craniosynostosis Crouzon Syndrome with Acanthosis Nigricans Cryoglobulinemia Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Duodenitis Dysfibrinogenemia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Classic Type, 1 Endometriosis Endotheliitis Epithelial-Myoepithelial Carcinoma Erythromelalgia Essential Thrombocythemia Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature 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 Femoral Neuropathy Fournier Gangrene Genitopatellar Syndrome Giant Hemangioma Gingivitis Glanzmann Thrombasthenia Glycogen Storage Disease Hantavirus Pulmonary Syndrome Hellp Syndrome Hemangioma Hemarthrosis Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemophilic Arthropathy Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hereditary Hemorrhagic Telangiectasia Human Immunodeficiency Virus Type 1 Hypercholesterolemia, Autosomal Dominant, 3 Immune System Disease Immunoglobulin E Concentration, Serum Infiltrating Lipoma Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Juvenile Hereditary Hemochromatosis Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Lupus Erythematosus Lymphangioma Lymphoma Macular Dystrophy, Retinal, 1, North Carolina Type Madelung Deformity Mallory-Weiss Syndrome Mayer-Rokitansky-Kuster-Hauser Syndrome Mild Hemophilia a Mixed Connective Tissue Disease Mononeuropathy of the Median Nerve, Mild Myelofibrosis Myocardial Infarction Necrotizing Ulcerative Gingivitis Neuropathy Nonarteritic Anterior Ischemic Optic Neuropathy Norrie Disease Ovarian Hyperstimulation Syndrome Paracetamol Poisoning Paracoccidioidomycosis Pericardial Effusion Periodontitis Peripheral Vertigo Platelet Aggregation, Spontaneous Platelet Factor 3 Deficiency Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Primary Thrombocytopenia Prostatitis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudo-Von Willebrand Disease Psychotic Disorder Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Renal Glucosuria Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Scoliosis Scott Syndrome Seizure Disorder Severe Hemophilia a Severe Hemophilia B Sickle Cell Disease Sneddon Syndrome Spinal Cord Infarction Stormorken Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thrombotic Thrombocytopenic Purpura, Acquired Thyroiditis Turner Syndrome Uremia Varicose Veins Vein Disease Venous Insufficiency Vitamin K Deficiency Hemorrhagic Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3 Wilms Tumor 6 Wilson-Turner X-Linked Mental Retardation Syndrome