Informaţii despre

Nume Antithrombin Iii Deficiency
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Primary Thrombophilia
Clasificare anatomică Malacards Boli de sânge; Boli osoase

Vezi şi

Boli A-Z Acanthamoeba Keratitis Acquired Angioedema Acquired Hemophilia Acute Liver Failure Acute Promyelocytic Leukemia Adie Pupil Afibrinogenemia Afibrinogenemia, Congenital Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amyloidosis Andersen Cardiodysrhythmic Periodic Paralysis Angioedema Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Arterial Tortuosity Syndrome Arteries, Anomalies of Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia-Telangiectasia Atrial Fibrillation Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Burns Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Chromosomal Triplication Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Cryptogenic Cirrhosis Diabetes Mellitus Disseminated Intravascular Coagulation Dysfibrinogenemia Eclampsia Endocarditis End Stage Renal Failure Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Fournier Gangrene Giant Hemangioma Glomerulonephritis Hellp Syndrome Hemoglobin E Disease Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatitis Hereditary Antithrombin Deficiency Homocysteinemia Homocystinuria Hypersplenism Ichthyosis Bullosa of Siemens Immune System Disease Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Laryngeal Cleft Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Lupus Erythematosus Lymphoblastic Leukemia Marantic Endocarditis May-Thurner Syndrome Meningococcemia Mesenteric Vascular Occlusion Mosaic Trisomy 8 Musical Perfect Pitch Myelodysplastic Syndrome Myocardial Infarction Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Ovarian Hyperstimulation Syndrome Papilledema Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Pneumonia Porencephaly Portal Vein Thrombosis 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 Quebec Platelet Disorder Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Severe Pre-Eclampsia Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombasthenia Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Toxic Shock Syndrome Varicose Veins Vascular Hemostatic Disease Vasculitis Vein Disease Von Willebrand's Disease