Informaţii despre

Nume Stroke, Ischemic
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic; Cerebral infarction due to embolism of cerebral arteries; Cerebral infarction due to embolism of precerebral arteries; Cerebral infarction due to thrombosis of cerebral arteries; Cerebral infarction due to thrombosis of precerebral arteries; Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries; Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries; Cerebral infarction, unspecified
Clasificare anatomică Malacards Boli cardiovasculare

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Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency Abcd Syndrome Acanthamoeba Keratitis Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acute Anterolateral Myocardial Infarction Acute Chest Syndrome Acute Cor Pulmonale Acute Mountain Sickness Acute Myocardial Infarction Acute Pancreatitis Acute Posterior Multifocal Placoid Pigment Epitheliopathy Acute Pulmonary Heart Disease Adenocarcinoma Adenomyosis Adenosine Deaminase 2 Deficiency Adult Respiratory Distress Syndrome Afibrinogenemia Afibrinogenemia, Congenital Aganglionosis, Total Intestinal Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amusia Anca-Associated Vasculitis Aneurysm Angina Pectoris Angiokeratoma of Fordyce Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Anuria Aortic Atherosclerosis Aortic Coarctation Aplastic Anemia Apraxia Arcus Corneae Argentine Hemorrhagic Fever Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arterial Thoracic Outlet Syndrome Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Asplenia, Isolated Congenital Atherosclerosis Susceptibility Atrial Fibrillation Atrial Septal Aneurysm Atrial Septal Defect 4 Auriculocondylar Syndrome 1 Axonal Neuropathy Bacterial Meningitis Basilar Artery Occlusion B-Cell Lymphomas Bipolar Disorder Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Edema Brain Injury Brain Ischemia Branch Retinal Artery Occlusion Breast Cancer Budd-Chiari Syndrome Buerger Disease Capgras Syndrome Capillary Leak Syndrome Carotid Artery Disease Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Stenosis Castleman Disease Cataract 5, Multiple Types Catastrophic Antiphospholipid Syndrome Cavernous Sinus Thrombosis Central Nervous System Lymphoma Central Nervous System Tuberculosis Central Neurocytoma Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Aneurysms Cerebral Arterial Disease Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Atrophy Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cervical Rib Cervicitis Cholesterol Embolism Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Meningitis Chronic Venous Insufficiency Churg-Strauss Syndrome Clopidogrel Resistance Cocaine Abuse Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conjugate Gaze Palsy Coronary Artery Aneurysm Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Coronary Thrombosis Cortical Blindness Cranial Nerve Palsy Cranioectodermal Dysplasia 1 Cryptococcal Meningitis Cryptogenic Cirrhosis Defective Apolipoprotein B-100 Dementia Diabetes Mellitus Diabetic Angiopathy Diarrhea Diastolic Heart Failure Dilated Cardiomyopathy Disseminated Intravascular Coagulation Dysbaric Osteonecrosis Dysfibrinogenemia Dystonia Echolalia Eclampsia Eisenmenger Syndrome Encephalitis Encephalomyopathy Encephalopathy Endocarditis Endometrial Stromal Sarcoma Endotheliitis Eosinophilic Granulomatosis with Polyangiitis Erythromelalgia Essential Thrombocythemia Exfoliation Syndrome Fabry Disease Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Familial Hyperlipidemia Fanconi Anemia, Complementation Group E Fasciitis Femoral Neuropathy Fibrinolytic Defect Fibromuscular Dysplasia Focal Dystonia Foix Chavany Marie Syndrome Foot Drop Fournier Gangrene Ganglioglioma Gastroduodenitis Gastrointestinal Stromal Tumor Giant Hemangioma Glanzmann Thrombasthenia Glucose Intolerance Gray Platelet Syndrome Headache Head Injury Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemifacial Atrophy, Progressive Hemiplegia Hemoglobinopathy Hemoglobinuria Hemolytic-Uremic Syndrome Hemophilia Hemophilia a Hemophilia B Hemorrhage, Intracerebral Hemorrhagic Disease Hemorrhagic Shock and Encephalopathy Syndrome Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatorenal Syndrome Hereditary Spherocytosis Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Herpes Zoster Ophthalmicus Homocysteinemia Homocystinuria Homozygous Familial Hypercholesterolemia Hydranencephaly Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hypereosinophilic Syndrome Hyperglycemia Hyperlexia Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertensive Nephropathy Hypertensive Retinopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoglycemia Hypolipoproteinemia Hypoparathyroidism Hyporeninemic Hypoaldosteronism Hypoxia Immune System Disease Immunoglobulin E Concentration, Serum Infective Endocarditis Inferior Vena Cava Interruption Inherited Blood Coagulation Disease Inherited Metabolic Disorder Intermittent Claudication Interstitial Nephritis Intestinal Impaction Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Intracranial Hypotension Intracranial Sinus Thrombosis Intracranial Thrombosis Intracranial Vasospasm Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Intravascular Large B-Cell Lymphoma Ischemia Ischemic Colitis Ischemic Heart Disease Ischemic Neuropathy Ischemic Optic Neuropathy Kearns-Sayre Syndrome Kleine-Levin Hibernation Syndrome Klippel-Trenaunay-Weber Syndrome Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Leukemia Leukodystrophy, Hypomyelinating, 3 Leukomalacia Ligneous Conjunctivitis Lipid Metabolism Disorder Lipoprotein Glomerulopathy Livedoid Vasculopathy Loeffler Endocarditis Logopenic Progressive Aphasia Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Malaria Malignant Atrophic Papulosis Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Marantic Endocarditis May-Hegglin Anomaly May-Thurner Syndrome Melkersson-Rosenthal Syndrome Meningitis Meningococcal Meningitis Meningococcemia Meningoencephalitis Menkes Disease Mesenteric Vascular Occlusion Microscopic Polyangiitis Middle Cerebral Artery Infarction Migraine with Aura Miller Fisher Syndrome Mini Stroke Mitochondrial Encephalomyopathy Mitral Valve Disease Mitral Valve Stenosis Moderate and Severe Traumatic Brain Injury Mucositis Muscular Dystrophy Myelitis Myelodysplastic Syndrome Myocardial Infarction Myocardial Stunning Necrotizing Fasciitis Neonatal Abstinence Syndrome Neonatal Stroke Nephrosclerosis Nephrotic Syndrome Neurilemmoma Neuroaxonal Dystrophy Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neurosyphilis Neutrophil Actin Dysfunction Nonarteritic Anterior Ischemic Optic Neuropathy Non-Involuting Congenital Hemangioma Occlusion Precerebral Artery Optic Nerve Neoplasm Osteonecrosis Ovarian Cancer Ovarian Hyperstimulation Syndrome Pancreatitis Paracetamol Poisoning Paragonimiasis Paroxysmal Cold Hemoglobinuria Patent Foramen Ovale Peripheral Artery Disease Peripheral Vertigo Peritonitis Persistent Vegetative State Pheochromocytoma Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Apoplexy Placenta Disease Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Plasmodium Vivax Malaria Platelet Aggregation, Spontaneous Platelet Membrane Fluidity Pleuropulmonary Blastoma Pneumococcal Meningitis Pneumonia Poems Syndrome Polyarteritis Nodosa Polycythemia Polyneuropathy Polyradiculoneuropathy Porencephaly Portal Hypertension Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Premature Menopause Prosopagnosia Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Artery Leiomyosarcoma Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Purpura Purpura Fulminans Qualitative Platelet Defect Quebec Platelet Disorder Radiculopathy Raynaud Disease Renal Artery Disease Renal Artery Obstruction Renal Dysplasia Renal Fibrosis Renal Hypertension Renal Tubular Dysgenesis Renovascular Hypertension Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Reversible Cerebral Vasoconstriction Syndrome Rheumatic Heart Disease Riboflavin Deficiency Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Sarcoma Scheie Syndrome Scotoma Scrub Typhus Sebastian Syndrome Sickle Cell Anemia Sickle Cell Disease Sinusitis Sleep Apnea Sneddon Syndrome Sphenoid Sinusitis Spinal Cord Infarction Spondyloocular Syndrome Spontaneous Intracranial Hypotension Spotted Fever Status Epilepticus Sticky Platelet Syndrome Sturge-Weber Syndrome Subacute Bacterial Endocarditis Subdural Empyema Subendocardial Myocardial Infarction Subependymoma Sudden Sensorineural Hearing Loss Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Systemic Scleroderma Tangier Disease Temporal Arteritis Testicular Germ Cell Cancer Tetralogy of Fallot Thalassemia Thoracic Outlet Syndrome Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thunderclap Headache Thyroid Crisis Thyroiditis Thyroid Lymphoma Toxocariasis Transient Cerebral Ischemia Transient Global Amnesia Traumatic Brain Injury Triple X Syndrome Tuberculous Meningitis Ulcerative Colitis Unilateral Absence of a Pulmonary Artery Uremia Ureteral Disease Van Der Woude Syndrome 1 Varicose Veins Vascular Dementia Vascular Disease Vasculitis Vein Disease Venous Insufficiency Vestibular Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Wallerian Degeneration Weber Syndrome Wolff-Parkinson-White Syndrome Xanthoma Disseminatum Xanthomatosis