Informaţii despre

Nume Factor Viii Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Hereditary factor VIII deficiency

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Liver Failure Acute Myocardial Infarction Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antithrombin Iii Deficiency Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Platelet Disease Budd-Chiari Syndrome Cardiac Tamponade Carotid Artery Occlusion Central Retinal Vein Occlusion Cerebral Arteritis Cerebral Sinovenous Thrombosis Cohen-Gibson Syndrome Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Ehlers-Danlos Syndrome Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xiii Deficiency Fainting Fournier Gangrene Glanzmann Thrombasthenia Graves' Disease Hellp Syndrome Hemarthrosis Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemophilic Arthropathy Hemorrhagic Disease Hepatic Adenomas, Familial Hyper Ige Syndrome Immunoglobulin E Concentration, Serum Inherited Blood Coagulation Disease Intermittent Claudication Intracranial Thrombosis Ischemic Colitis Korean Hemorrhagic Fever Livedoid Vasculopathy Mediastinitis Mild Hemophilia a Myocardial Infarction Nonarteritic Anterior Ischemic Optic Neuropathy Paine Syndrome Paracetamol Poisoning Peripheral Vertigo Placental Abruption Polyradiculoneuropathy Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Purpura Qualitative Platelet Defect Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Rheumatoid Arthritis Sagittal Sinus Thrombosis Scott Syndrome Severe Hemophilia a Sneddon Syndrome Spinal Cord Infarction Spotted Fever Stroke, Ischemic Sudden Sensorineural Hearing Loss Synovitis 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 X-Linked Disease