Informaţii despre

Nume Retinal Vascular Occlusion
Pagina Web www.malacards.org
Clasificari ICD10 Retinal vascular occlusion, unspecified
Clasificare anatomică Malacards Boli ale ochiului; Boli cardiovasculare

Vezi şi

Boli A-Z Acanthamoeba Keratitis Acute Liver Failure Afibrinogenemia Afibrinogenemia, Congenital Alpha-2-Plasmin Inhibitor Deficiency Al-Raqad Syndrome Amaurosis Fugax Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arteritic Anterior Ischemic Optic Neuropathy Atrial Fibrillation Basilar Artery Occlusion Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Globoside System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Cancer-Associated Retinopathy Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebrovascular Disease Chickenpox Choroiditis Chronic Myocardial Ischemia Corneal Neovascularization Cryptogenic Cirrhosis Degenerative Myopia Diabetic Angiopathy Diabetic Macular Edema Disseminated Intravascular Coagulation Dysfibrinogenemia Eclampsia Ectopic Pregnancy Endocarditis Endophthalmitis Epithelioid Hemangioendothelioma Esophageal Varix Exfoliation Syndrome Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Fanconi Anemia, Complementation Group G Femoral Neuropathy Fournier Gangrene Giant Hemangioma Glanzmann Thrombasthenia Hellp Syndrome Hemifacial Spasm Hemiplegia Hemoglobin E Disease Hemoglobinuria Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Homocysteinemia Homocystinuria Hypersplenism Immune System Disease Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Kuhnt-Junius Degeneration Lateral Medullary Syndrome Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Livedoid Vasculopathy Lupus Erythematosus Macular Holes Macular Retinal Edema Marantic Endocarditis May-Thurner Syndrome Meningococcemia Mesenteric Vascular Occlusion Mitral Valve Stenosis Neovascular Glaucoma Nephrosclerosis Neuropathy Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Ovarian Hyperstimulation Syndrome Papilledema Paracetamol Poisoning Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Peliosis Hepatis Peripheral Artery Disease Peripheral Vertigo Placenta Disease Placental Abruption Placental Insufficiency Platelet Aggregation, Spontaneous 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 Qualitative Platelet Defect Quebec Platelet Disorder Retinal Artery Occlusion Retinal Vascular Disease Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Severe Pre-Eclampsia Sickle Cell Disease Sneddon Syndrome Spinal Cord Infarction Splenic Infarction Sticky Platelet Syndrome Stormorken Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Varicose Veins Vascular Disease Vasculitis Vein Disease Venous Insufficiency Vitreous Detachment Vitreous Disease Von Willebrand's Disease