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Nume Thrombophilia Due to Activated Protein C Resistance
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificare anatomică Malacards Blood diseases
Boli din aceeaşi familie Thrombophilia Due to Thrombin Defect; Thrombophilia Due to Thrombomodulin Defect; Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator

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Boli A-Z Acanthamoeba Keratitis Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Cor Pulmonale Acute Liver Failure Acute Myocardial Infarction Acute Poststreptococcal Glomerulonephritis Acute Pulmonary Heart Disease Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Amaurosis Fugax Angina Pectoris Aniridia 1 Anomalous Left Coronary Artery from the Pulmonary Artery Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Anteroseptal Myocardial Infarction Antiphospholipid Syndrome Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Basilar Artery Occlusion Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Breast Reconstruction Budd-Chiari Syndrome Buerger Disease Cardiac Tamponade Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebral Arteritis Cerebral Falx Meningioma Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebrovascular Disease Cold Urticaria Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Ia Conjugate Gaze Palsy Coronary Thrombosis Cryptogenic Cirrhosis Diabetic Angiopathy Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Eclampsia Eisenmenger Syndrome Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Epileptic Encephalopathy, Childhood-Onset Essential Thrombocythemia Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor V Leiden Thrombophilia Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Femoral Neuropathy Fibrinolytic Defect Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Hellp Syndrome Hemarthrosis Hemoglobin E Disease Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Homocysteinemia Homocystinuria Immune System Disease Infective Endocarditis Inferior Myocardial Infarction Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Kwashiorkor Lateral Medullary Syndrome Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Ligneous Conjunctivitis Livedoid Vasculopathy Marantic Endocarditis May-Thurner Syndrome Meningococcemia Mercury Poisoning Mesenteric Vascular Occlusion Mild Hemophilia a Mitral Valve Stenosis Neonatal Stroke Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Papilledema Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Porencephaly Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Posterior Myocardial Infarction Posterolateral Myocardial Infarction Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Raynaud Disease Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Severe Hemophilia a Severe Hemophilia B Severe Pre-Eclampsia Shwartzman Phenomenon Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Spotted Fever Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Thoracic Outlet Syndrome Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Thrombin Defect Thrombophilia Due to Thrombomodulin Defect Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Tuberculous Empyema Unilateral Absence of a Pulmonary Artery Varicose Veins Vascular Disease Vascular Hemostatic Disease Vasculitis 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