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Nume Varicose Veins
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Clasificare anatomică Malacards Boli cardiovasculare

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Boli A-Z Acute Myocardial Infarction Adenomyosis Adult Astrocytic Tumour Afibrinogenemia Afibrinogenemia, Congenital Aging Al Amyloidosis Alcoholic Liver Cirrhosis Alpha-2-Plasmin Inhibitor Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Amaurosis Fugax Androgen Insensitivity Syndrome, Mild Aneurysm Angiodysplasia Angiokeratoma Circumscriptum Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm, Familial Abdominal, 1 Aortic Aneurysm, Familial Thoracic 1 Aortic Disease Appendix Adenocarcinoma Arteries, Anomalies of Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Axenfeld-Rieger Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharochalasis Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Platelet Disease Blood Protein Disease 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 Glioblastoma Multiforme Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Burns Carotid Artery Disease Carotid Stenosis Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cholesteatoma of Middle Ear Chromoblastomycosis Chronic Actinic Dermatitis Chronic Venous Insufficiency Chronic Venous Leg Ulcers Collagen Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Conjunctival Nevus Conjunctivochalasis Corneal Ulcer Coronary Artery Aneurysm Crouzon Syndrome with Acanthosis Nigricans Cryptogenic Cirrhosis Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Dysfibrinogenemia Eclampsia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Vascular Type Elephantiasis Endotheliitis Epidermolysis Bullosa Dystrophica Epileptic Encephalopathy, Childhood-Onset Exfoliation Syndrome Exophthalmos Extracranial Arteriovenous Malformation Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Familial Abdominal Aortic Aneurysm Fasciitis Fibromatosis, Gingival, 1 Fibrosarcoma Focal Myositis Foot Drop Fournier Gangrene Gingival Fibromatosis Gingival Hypertrophy Gingival Overgrowth Hellp Syndrome Hemifacial Spasm Hemoglobin E Disease Hemophilia a Hemorrhagic Disease Hemorrhoid Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatitis Hepatitis C Hepatitis C Virus Hepatoportal Sclerosis Homocysteinemia Homocystinuria Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypotonia-Cystinuria Syndrome Hypotrichosis Hypoxia Immune System Disease Inferior Vena Cava Interruption Infiltrating Angiolipoma Inguinal Hernia Inherited Blood Coagulation Disease Intermittent Claudication Intermittent Proptosis Internal Hemorrhoid Intestinal Impaction Intracranial Hypertension Intracranial Thrombosis Intravascular Papillary Endothelial Hyperplasia Ischemic Colitis Ischemic Optic Neuropathy Kagami-Ogata Syndrome Kaufman Oculocerebrofacial Syndrome Kawasaki Disease Klippel-Trenaunay-Weber Syndrome Korean Hemorrhagic Fever Kwashiorkor Leech Infestation Leiomyoma Lentigo Maligna Melanoma Light Chain Deposition Disease Limb Ischemia Lipedema Lipodermatosclerosis Livedoid Vasculopathy Liver Cirrhosis Lower Limb Hypertrophy Lung Giant Cell Carcinoma Lymphangioleiomyomatosis Lymphedema Malignant Glioma Marantic Endocarditis Mesenteric Vascular Occlusion Microcystic Meningioma Mid-Dermal Elastolysis Myocardial Infarction Nasal Cavity Squamous Cell Carcinoma Necrotizing Fasciitis Neuropathy Nodular Malignant Melanoma Nonarteritic Anterior Ischemic Optic Neuropathy Odontogenic Myxoma Oral Squamous Cell Carcinoma Osteonecrosis Paracetamol Poisoning Parotitis Patent Foramen Ovale Pelvic Organ Prolapse Periodontal Disease Periodontitis Peripheral Vertigo Peroneal Neuropathy Pituitary Adenoma 1, Multiple Types Placenta Disease Placental Abruption Plasminogen Deficiency, Type I Platelet Aggregation, Spontaneous Plica Syndrome Pneumothorax Porencephaly Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Proteus Syndrome Prothrombin Deficiency Prothrombin Deficiency, Congenital Psammomatous Meningioma Pulmonary Embolism Pulmonary Emphysema Purpura Purpura Fulminans Qualitative Platelet Defect Ramer Ladda Syndrome Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Rheumatoid Nodulosis Sagittal Sinus Thrombosis Salivary Gland Cancer Sarcoma Senile Ectropion Sensorineural Hearing Loss Septic Arthritis Severe Pre-Eclampsia Sick Building Syndrome Sneddon Syndrome Sorsby Fundus Dystrophy Sparganosis Spastic Entropion Spinal Cord Infarction Spinal Stenosis Squamous Cell Carcinoma, Head and Neck Squamous Cell Carcinoma of the Hypopharynx Sticky Platelet Syndrome Stroke, Ischemic Sturge-Weber Syndrome Sudden Sensorineural Hearing Loss Superior Limbic Keratoconjunctivitis Supravalvular Aortic Stenosis Takayasu Arteritis Taylor's Syndrome Tendinosis Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Undifferentiated Pleomorphic Sarcoma Varicocele Vascular Disease Vein Disease Venous Insufficiency Villous Adenocarcinoma Von Willebrand's Disease Von Willebrand Disease, Type 1 Weber Syndrome Wrinkles