Informaţii despre

Nume Peripheral Vertigo
Pagina Web www.malacards.org
Clasificari ICD10 Other peripheral vertigo
Clasificare anatomică Malacards Boli ale urechii

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Boli A-Z Acanthamoeba Keratitis Acquired Angioedema Acquired Hemophilia Acquired Hemophilia a Acute Liver Failure Acute Myocardial Infarction Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alpha-2-Plasmin Inhibitor Deficiency Analbuminemia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteritic Anterior Ischemic Optic Neuropathy Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Bronchus Cancer Budd-Chiari Syndrome Buerger Disease Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Nervous System Origin Vertigo Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Coronary Thrombosis Cryptogenic Cirrhosis Deafness, Autosomal Dominant 6 Deafness, Autosomal Dominant 9 Deafness, Autosomal Recessive 16 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct Dental Abscess Diabetes Insipidus Diabetes Insipidus, Nephrogenic, Autosomal Diabetes Insipidus, Neurohypophyseal Disseminated Intravascular Coagulation Dysfibrinogenemia Endocarditis Endocardium Disease Esophageal Varix Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fournier Gangrene Gastroesophageal Reflux Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Headache Hellp Syndrome 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 Hepatorenal Syndrome Homocysteinemia Homocystinuria Hypersplenism Immune System Disease Impaired Renal Function Disease Inappropriate Adh Syndrome Infective Endocarditis Inherited Blood Coagulation Disease Inner Ear Disease Intermediate Coronary Syndrome Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Japanese Spotted Fever Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Malignant Otitis Externa Marantic Endocarditis Mastoiditis May-Thurner Syndrome Mediastinitis Meniere Disease Meningococcemia Motion Sickness Nonarteritic Anterior Ischemic Optic Neuropathy Papilledema Paracetamol Poisoning Patent Foramen Ovale Pendred Syndrome Placenta Disease Placental Abruption Plexopathy Polyarteritis Nodosa Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Edema Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Scott Syndrome Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Severe Hemophilia a Severe Pre-Eclampsia Sneddon Syndrome Spinal Cord Infarction Splenic Disease Splenic Infarction Sticky Platelet Syndrome Stiff-Person Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Syndrome of Inappropriate Antidiuretic Hormone Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Varicose Veins Vein Disease Vestibular Disease Von Willebrand's Disease Von Willebrand Disease, Type 1