Informaţii despre

Nume Factor V Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Hereditary deficiency of other clotting factors
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acquired Von Willebrand Syndrome Acute Liver Failure Adenocarcinoma Afibrinogenemia Afibrinogenemia, Congenital Aging Al Amyloidosis Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Analbuminemia Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Platelet Disease Blue Toe Syndrome Budd-Chiari Syndrome Buerger Disease Bullous Pemphigoid Burns Cardiac Tamponade Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Coronary Artery Anomaly Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Dysfibrinogenemia Factor V and Factor Viii, Combined Deficiency of, 2 Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fournier Gangrene Gastric Cancer Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Hemarthrosis Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hepatic Adenomas, Familial Hepatic Infarction Hereditary Spherocytosis Infertility Inherited Blood Coagulation Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Korean Hemorrhagic Fever Leech Infestation Leukemia Livedoid Vasculopathy Marantic Endocarditis Mesenteric Vascular Occlusion Myeloproliferative Neoplasm Neurodegeneration with Brain Iron Accumulation 2a Nonarteritic Anterior Ischemic Optic Neuropathy Ovarian Cyst Paracetamol Poisoning Peripheral Vertigo Placental Abruption Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Tuberculosis Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Rapp-Hodgkin Syndrome Retinal Artery Occlusion Retinal Vascular Occlusion Rheumatoid Arthritis Ring Chromosome 2 Sagittal Sinus Thrombosis Sarcoma Scott Syndrome Severe Hemophilia a Severe Hemophilia B Sneddon Syndrome Spinal Cord Infarction Splenic Disease Stroke, Ischemic Sudden Sensorineural Hearing Loss Thalassemia Thrombasthenia Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Vein Disease Ventricular Septal Defect Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2