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Nume Cerebrovascular Disease
Pagina Web www.malacards.org
Clasificari ICD10 Cerebral infarction, unspecified; Cerebrovascular disease, unspecified; Other specified cerebrovascular diseases
Clasificare anatomică Malacards Boli cardiovasculare

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Boli A-Z Aarskog-Scott Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acquired Angioedema Acquired Metabolic Disease Acrocallosal Syndrome Actinic Prurigo Acute Adrenal Insufficiency Acute Liver Failure Acute Myocardial Infarction Acute Pyelonephritis Acute Respiratory Distress Syndrome Acute Transverse Myelitis Adult-Onset Still's Disease Adult Respiratory Distress Syndrome Afibrinogenemia Afibrinogenemia, Congenital Aganglionosis, Total Intestinal Aging Alcoholic Hepatitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Angiolipoma Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortic Atherosclerosis Aortic Disease Apnea, Obstructive Sleep Appendicitis Apraxia Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspiration Pneumonia Aspirin Resistance Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Atrial Fibrillation Atrial Septal Defect 4 Atrichia with Papular Lesions Autoimmune Hepatitis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Bacterial Meningitis Basilar Artery Occlusion Bernard-Soulier Syndrome Binswanger's Disease Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet 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 Brain Edema Brain Injury Bronchiolitis Obliterans Budd-Chiari Syndrome Buerger Disease Bullous Pemphigoid Burns Cardiogenic Shock Carotid Artery Disease Carotid Artery Thrombosis Carotid Stenosis Catastrophic Antiphospholipid Syndrome Central Nervous System Vasculitis Central Retinal Vein Occlusion Cerebral Atherosclerosis Cerebral Atrophy Cerebral Palsy Cerebritis Charles Bonnet Syndrome Chlamydia Cholangitis Chorioamnionitis Chronic Venous Insufficiency Citrullinemia, Classic Clopidogrel Resistance Cognitive Function 1, Social Cold Agglutinin Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Conotruncal Heart Malformations Contact Dermatitis Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Coronary Thrombosis Crescentic Glomerulonephritis Critical Illness Polyneuropathy Cryptogenic Cirrhosis Cutaneous Lupus Erythematosus Cytomegalovirus Infection Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Defective Apolipoprotein B-100 Delusional Disorder Dementia De Sanctis-Cacchione Syndrome Diabetes Mellitus Diabetic Angiopathy Diabetic Foot Ulcers Dirofilariasis Disseminated Intravascular Coagulation Diverticulitis Duodenal Ulcer Dwarfism Dysbaric Osteonecrosis Dysfibrinogenemia Ehlers-Danlos Syndrome Endocarditis Endometritis Endotheliitis End Stage Renal Failure Epilepsy Epilepsy, Partial, with Pericentral Spikes Fabry Disease Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Familial Hyperlipidemia Familial Lcat Deficiency Fetal Macrosomia Fibrinolytic Defect Fibromuscular Dysplasia Gait Apraxia Gallbladder Disease Gastroschisis Gingivitis Glanzmann Thrombasthenia Glucose Metabolism Disease Glucosephosphate Dehydrogenase Deficiency Glycine N-Methyltransferase Deficiency Glycogen Storage Disease Graves' Disease Growth Control, Y-Chromosome Influenced Headache Heart Cancer Heart Conduction Disease Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemoglobin E Disease Hemophilia Hemophilia a Hemorrhage, Intracerebral Hemorrhagic Disease Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hepatic Encephalopathy Hepatic Lipase Deficiency Hepatic Vascular Disease Hepatitis Hepatitis C Hepatitis C Virus Hepatoportal Sclerosis Hepatorenal Syndrome Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homozygous Familial Hypercholesterolemia Hutchinson-Gilford Progeria Syndrome Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperglycemia Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypersensitivity Reaction Type Iii Disease Hypertension, Diastolic Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hypertensive Retinopathy Hypertriglyceridemia, Familial Hyperuricemia Hypoaldosteronism Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypoganglionosis Hypolipoproteinemia Hypopituitarism Hyporeninemic Hypoaldosteronism Hypoxia Idiopathic Edema Immune-Complex Glomerulonephritis Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Infertility Influenza Inherited Blood Coagulation Disease Inherited Metabolic Disorder Intermittent Claudication Internuclear Ophthalmoplegia Interstitial Nephritis Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Intracranial Vasospasm Ischemia Ischemic Colitis Ischemic Heart Disease Ischemic Neuropathy Ischemic Optic Neuropathy Isolated Growth Hormone Deficiency, Type Ia Kawasaki Disease Koro Laryngeal Cleft Lateral Medullary Syndrome Lecithin:cholesterol Acyltransferase Deficiency Legg-Calve-Perthes Disease Lemierre's Syndrome Lens Subluxation Leptospirosis Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukostasis Leukotriene C4 Synthase Deficiency Limb Ischemia Lipid Metabolism Disorder Lipodystrophy, Partial, Acquired Lipoprotein Glomerulopathy Livedoid Vasculopathy Localized Scleroderma Louse-Borne Relapsing Fever Lupus Erythematosus Lutheran Suppressor, X-Linked Lyme Disease Lymphocytic Vasculitis Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Marantic Endocarditis Marfan Syndrome Mast Cell Activation Syndrome Mastoiditis Mediastinitis Megacolon Meningitis Mesenteric Vascular Occlusion Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii Microscopic Polyangiitis Microvascular Complications of Diabetes 1 Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Migraine with Aura Mini Stroke Moderate and Severe Traumatic Brain Injury Mood Disorder Mooren's Ulcer Mucopolysaccharidosis, Type Vii Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Chemical Sensitivity Multiple Symmetrical Lipomatosis Myelomeningocele Myocardial Infarction Neonatal Stroke Nephrosclerosis Nervous System Disease Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neutrophil Actin Dysfunction Nevus Comedonicus Noma Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Osteonecrosis Osteoporotic Fracture Osteosclerotic Myeloma Overnutrition Pancreatitis Paracetamol Poisoning Patent Foramen Ovale Pericardial Effusion Pericarditis Perinatal Necrotizing Enterocolitis Periodontal Disease Periodontitis Peripheral Artery Disease Peripheral Vertigo Peritonitis Pituitary Tumors Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Plasmodium Vivax Malaria Platelet Aggregation, Spontaneous Pleurisy Pneumonia Polyarteritis Nodosa Polydactyly, Postaxial, with Progressive Myopia Polyneuropathy Porencephaly Portal Hypertension Portal Vein Thrombosis Posterior Urethral Valves Post-Thrombotic Syndrome Prediabetes Syndrome Pregnancy Loss, Recurrent 1 Primary Cerebellar Degeneration Primary Progressive Multiple Sclerosis Primary Thrombocytopenia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudohypoparathyroidism Psoriasis Psoriasis 13 Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Sarcoidosis Pure Autonomic Failure Purpura Pyelonephritis Qualitative Platelet Defect Quebec Platelet Disorder Reactive Arthritis Relapsing-Remitting Multiple Sclerosis Renal Artery Disease Renal Artery Obstruction Renal Dysplasia Renal Hypertension Renal Tubular Dysgenesis Renovascular Hypertension Restless Legs Syndrome Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Reunion Island Larsen Syndrome Rheumatic Disease Rheumatic Heart Disease Rheumatoid Arthritis Rheumatoid Vasculitis Riboflavin Deficiency Rosacea Scalp-Ear-Nipple Syndrome Schizencephaly Scleritis Scorpion Envenomation Scott Syndrome Senile Plaque Formation Sensorineural Hearing Loss Severe Pre-Eclampsia Shwartzman Phenomenon Sickle Cell Anemia Sickle Cell Disease Sleep Apnea Sneddon Syndrome Spinal Cord Infarction Spinocerebellar Degeneration Spondylitis Spondyloarthropathy 1 Spotted Fever Stroke, Ischemic Subacute Cutaneous Lupus Erythematosus Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Supranuclear Palsy, Progressive, 1 Synovitis Systemic Lupus Erythematosus Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Tangier Disease Taqi Polymorphism Thalassemia Three M Syndrome 1 Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Transsexualism Transsexuality Transverse Myelitis Typhoid Fever Uremia Varicose Veins Vascular Dementia Vascular Disease Vasculitis Vein Disease Venous Insufficiency Viral Encephalitis Vitamin B12 Deficiency Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Wallerian Degeneration Xanthoma Disseminatum Xanthomatosis Zygomycosis