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Nume Vascular Disease
Pagina Web www.malacards.org
Clasificari ICD10 Aneurysm and dissection of unspecified site; Vascular dementia, unspecified; Vascular disorder of intestine, unspecified
Clasificare anatomică Malacards Boli cardiovasculare; Boli gastrointestinale; Boli neuronale; Boli psihice

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Abdominal Obesity-Metabolic Syndrome 1 Abetalipoproteinemia Acanthamoeba Keratitis Acanthosis Nigricans Achalasia-Addisonianism-Alacrima Syndrome Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acrocallosal Syndrome Acute Chest Syndrome Acute Mountain Sickness Acute Myocardial Infarction Adams-Oliver Syndrome Adhesive Otitis Media Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adrenocortical Carcinoma, Hereditary Afibrinogenemia, Congenital Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Amyloidosis Aa Anauxetic Dysplasia 1 Aneurysm Angina Pectoris Angiodysplasia Angioid Streaks Angiomatosis Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Aortic Aneurysm, Familial Abdominal, 1 Aortic Atherosclerosis Aortic Disease Aortic Valve Disease 2 Aortic Valve Insufficiency Aortitis Aortopulmonary Window Apnea, Obstructive Sleep Arachnoiditis Arcus Corneae Argentine Hemorrhagic Fever Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arterial Calcification, Generalized, of Infancy, 1 Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspirin Resistance Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Atrial Fibrillation Atrioventricular Septal Defect Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autonomic Neuropathy Bacteremia 2 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 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Edema Branch Retinal Artery Occlusion Breast Cancer Bronchopulmonary Dysplasia Budd-Chiari Syndrome Buerger Disease Carotid Artery Disease Carotid Artery Occlusion Carotid Artery Thrombosis Carotid Intimal Medial Thickness 2 Carotid Stenosis Carpal Tunnel Syndrome Cataract Catastrophic Antiphospholipid Syndrome Cauda Equina Syndrome Cavernous Malformation Central Retinal Vein Occlusion Cerebral Aneurysms Cerebral Atherosclerosis Cerebral Atrophy Cerebral Cavernous Malformations Cerebral Hypoxia Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cervicitis Charles Bonnet Syndrome Chlamydia Chorea, Childhood-Onset, with Psychomotor Retardation Chorea Gravidarum Choreatic Disease Chronic Pulmonary Heart Disease Chronic Thromboembolic Pulmonary Hypertension Chronic Ulcer of Skin Chronic Venous Insufficiency Colitis Collagen Disease Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Atrioventricular Canal Cone-Rod Dystrophy 2 Congestive Heart Failure Connective Tissue Disease Coronary Artery Aneurysm Coronary Artery Anomaly Coronary Artery Vasospasm Coronary Heart Disease 1 Coronary Restenosis Coronary Stenosis Coronary Thrombosis Costello Syndrome Critical Limb Ischemia Crouzon Syndrome with Acanthosis Nigricans Cryptogenic Cirrhosis Cytomegalovirus Infection Defective Apolipoprotein B-100 Dementia Dementia - Subcortical Dermatitis Developmental Coordination Disorder Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diabetic Autonomic Neuropathy Diabetic Cataract Diabetic Foot Ulcers Diabetic Macular Edema Diabetic Neuropathy Diastolic Heart Failure Diffuse Dermal Angiomatosis Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Diverticulitis Dysbaric Osteonecrosis Dyschromatosis Symmetrica Hereditaria Dysfibrinogenemia Earlobe Crease Eclampsia Eisenmenger Syndrome Encephalitis Endocarditis Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Epilepsy, Partial, with Pericentral Spikes Epileptic Encephalopathy, Childhood-Onset Erythromelalgia Essential Thrombocythemia Exfoliation Syndrome Factor X Deficiency Factor Xii Deficiency Factor Xiii Deficiency Familial Hyperlipidemia Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fatty Liver Disease Fibrinolytic Defect Fibrodysplasia Ossificans Progressiva Fibromuscular Dysplasia Frontotemporal Dementia Gallbladder Disease Gas Gangrene Genitopatellar Syndrome Gestational Diabetes Glucose Intolerance Glucose Metabolism Disease Gout Grange Syndrome Granulomatous Dermatitis Head Injury Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemifacial Spasm Hemophagocytic Lymphohistiocytosis Hemophilia a Hemorrhage, Intracerebral Hemorrhagic Disease Hemorrhagic Fever Hemosiderosis Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Lipase Deficiency Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis C Hepatoportal Sclerosis Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Herpes Zoster Heterotaxy Homocysteinemia Homocystinuria Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homozygous Familial Hypercholesterolemia Human Coronavirus Sensitivity 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 Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hypertensive Retinopathy Hypertriglyceridemia, Familial Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hyporeninemic Hypoaldosteronism Hypoxia Ichthyosis Prematurity Syndrome Idiopathic Edema Idiopathic Interstitial Pneumonia Idiopathic Recurrent Pericarditis Immune System Disease Impotence Inferior Vena Cava Interruption Inflammatory Bowel Disease Intermittent Claudication Interstitial Lung Disease Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Intracranial Vasospasm Ischemia Ischemic Colitis Ischemic Heart Disease Ischemic Optic Neuropathy Kawasaki Disease Lecithin:cholesterol Acyltransferase Deficiency Legg-Calve-Perthes Disease Lemierre's Syndrome Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukostasis Limb Ischemia Linear Scleroderma Lipid Metabolism Disorder Lipodermatosclerosis Lipodystrophy Lipoprotein Glomerulopathy Livedoid Vasculopathy Liver Disease Logopenic Progressive Aphasia Lung Cancer Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Malignant Essential Hypertension Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Malignant Secondary Hypertension Malignant Spiradenoma Marantic Endocarditis Marfan Syndrome May-Thurner Syndrome Meckel Syndrome, Type 1 Median Arcuate Ligament Syndrome Mediastinitis Melanoma Meningitis and Encephalitis Meningococcemia Meningoencephalitis Mesangial Proliferative Glomerulonephritis Microvascular Complications of Diabetes 1 Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Mild Pre-Eclampsia Mitral Valve Stenosis Mixed Connective Tissue Disease Moderate and Severe Traumatic Brain Injury Mononeuropathy of the Median Nerve, Mild Morbid Obesity Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Multiple Symmetrical Lipomatosis Muscular Dystrophy Mycosis Fungoides Myelomeningocele Myocardial Infarction Myocardial Stunning Neonatal Stroke Neovascular Glaucoma Nephrosclerosis Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neutropenia Neutrophil Actin Dysfunction Nonarteritic Anterior Ischemic Optic Neuropathy Nonspecific Interstitial Pneumonia Oliver Syndrome Osteomyelitis Osteonecrosis Ovarian Hyperstimulation Syndrome Overnutrition Pancreatitis Pancreatitis, Hereditary Papilledema Papillomatosis, Confluent and Reticulated Paraplegia Patent Foramen Ovale Pemphigus Pemphigus Vegetans Pemphigus Vulgaris Pericardial Effusion Periodontal Disease Periodontitis Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Peritonitis Placenta Disease Placental Abruption Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Platelet Membrane Fluidity Plica Syndrome Pneumonia Polyarteritis Nodosa Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Portal Hypertension Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Prediabetes Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Premature Chromatid Separation Trait Premature Menopause Prinzmetal's Variant Angina Prostatitis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudoxanthoma Elasticum Psoriasis Psoriasis 13 Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis Pulmonary Fibrosis, Idiopathic Pulmonary Hemosiderosis Pulmonary Hypertension Purpura Pyosalpinx Q Fever Qualitative Platelet Defect Quebec Platelet Disorder Raynaud Disease Recurrent Acute Pancreatitis Reflex Sympathetic Dystrophy Relapsing Polychondritis Renal Artery Disease Renal Artery Obstruction Renal Fibrosis Renal Hypertension Renal Hypodysplasia/aplasia 1 Renal Tuberculosis Renovascular Hypertension Resting Heart Rate, Variation in Restless Legs Syndrome Retinal Artery Occlusion Retinal Ischemia Retinal Vascular Disease Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinitis Rheumatoid Arthritis Rheumatoid Vasculitis Riboflavin Deficiency Rocky Mountain Spotted Fever Sagittal Sinus Thrombosis Scalp-Ear-Nipple Syndrome Schistosomiasis Schizophrenia Scleritis Serotonin Syndrome Severe Pre-Eclampsia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwartzman Phenomenon Sleep Apnea Smith-Lemli-Opitz Syndrome Smoking As a Quantitative Trait Locus 3 Sneddon Syndrome Spinal Cord Infarction Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Spotted Fever Sticky Platelet Syndrome St. Louis Encephalitis Stroke, Ischemic Subclavian Steal Syndrome Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Supraglottis Squamous Cell Carcinoma Supravalvular Aortic Stenosis Sveinsson Chorioretinal Atrophy Synovitis Systemic Lupus Erythematosus Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Tangier Disease Telangiectasis Temporal Arteritis Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombophlebitis Migrans Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toxic Oil Syndrome Transient Cerebral Ischemia Tropical Endomyocardial Fibrosis Ulcerative Colitis Unilateral Absence of a Pulmonary Artery Uremia Ureteral Disease Urinary System Disease Van Der Woude Syndrome 1 Varicose Veins Vascular Dementia Vasculitis Vein Disease Venous Insufficiency Viral Hemorrhagic Fever Viral Pneumonia Visceral Heterotaxy Vitamin B12 Deficiency Von Willebrand's Disease Williams-Beuren Syndrome Wrinkles Xanthoma Disseminatum Xanthomatosis