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Nume Aortic Aneurysm
Pagina Web www.malacards.org
Clasificari ICD10 Abdominal aortic aneurysm, ruptured; Aortic aneurysm of unspecified site, ruptured; Aortic aneurysm of unspecified site, without mention of rupture; Thoracic aortic aneurysm, ruptured; Thoracoabdominal aortic aneurysm, ruptured
Clasificare anatomică Malacards Boli cardiovasculare

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Boli A-Z Acalculous Cholecystitis Achalasia-Addisonianism-Alacrima Syndrome Acquired Cutis Laxa Acrocallosal Syndrome Acute Pancreatitis Acute Transverse Myelitis Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Aneurysm of Sinus of Valsalva Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Anuria Aorta-Pulmonary Artery Fistula Aortic Aneurysm, Familial Abdominal, 1 Aortic Aneurysm, Familial Thoracic 1 Aortic Aneurysm, Familial Thoracic 4 Aortic Coarctation Aortic Disease Aortic Valve Insufficiency Aortitis Aorto-Left Ventricular Tunnel Apert Syndrome Appendicitis Arterial Tortuosity Syndrome Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ascites, Chylous Aspergillus Niger Infection Ataxia Neuropathy Spectrum Atrioventricular Block Atrioventricular Septal Defect Autoimmune Pancreatitis Autosomal Dominant Polycystic Kidney Disease Ayme-Gripp Syndrome Back Pain Benign Adult Familial Myoclonic Epilepsy Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System 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 Bornholm Eye Disease Bronchiectasis Bronchiolitis Obliterans Bronchogenic Cyst Candidiasis Cantu Syndrome Cardiac Arrest Cardiac Tamponade Carotid Artery Disease Cauda Equina Syndrome Cerebellofaciodental Syndrome Cerebral Arterial Disease Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cervical Aortic Arch Cervicitis Char Syndrome Chlamydia Cholecystitis Cholelithiasis Cholesterol Embolism Chronic Actinic Dermatitis Chronic Mucocutaneous Candidiasis Chronic Venous Leg Ulcers Clostridium Septicum Infection Coarctation of Aorta Cogan Syndrome Colitis Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Conjunctival Nevus Conjunctivochalasis Connective Tissue Disease Constrictive Pericarditis Corneal Dystrophy, Fleck Coronary Artery Aneurysm Coronary Stenosis Craniosynostosis Critical Limb Ischemia Cutis Laxa Cutis Laxa, Autosomal Dominant 1 Cutis Laxa, Autosomal Recessive Type 1 Cutis Laxa, Autosomal Recessive, Type Ia Cystinosis Cytomegalovirus Infection Diabetes Mellitus Discitis Disseminated Intravascular Coagulation Diverticulitis Double Inferior Vena Cava Duodenal Obstruction Duodenitis Dysphagia Ehlers-Danlos Syndrome Encephalitis Encephalopathy Endotheliitis Epidural Abscess Exfoliation Syndrome Extracranial Arteriovenous Malformation Factor Vii Deficiency Familial Abdominal Aortic Aneurysm Familial Thoracic Aortic Aneurysm and Dissection Fanconi Anemia, Complementation Group E Femoral Neuropathy Fibromuscular Dysplasia Fibrosarcoma Fibrosclerosis, Multifocal Focal Myositis Fusariosis Galactosialidosis Gallbladder Cancer Gallbladder Disease Gastric Ulcer Gigantism Goiter Gonadal Dysgenesis Guillain-Barre Syndrome, Familial Haemophilus Influenzae Head Injury Hemangioma Heme Oxygenase 1 Deficiency Hemopericardium Hemophilia Hemophilia a Hemophilia B Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Coma Hepatitis Hepatocellular Carcinoma Hereditary Hemorrhagic Telangiectasia High Molecular Weight Kininogen Deficiency Hinman Syndrome Homocystinuria Horseshoe Kidney Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Scars Hypocalcemia, Autosomal Dominant 1 Hypoplastic Left Heart Syndrome Hypoxia Igg4-Related Disease Immunoglobulin E Concentration, Serum Impotence Inferior Myocardial Infarction Inflammatory Bowel Disease Influenza Inguinal Hernia Intermittent Claudication Interstitial Nephritis Intracranial Aneurysm Intracranial Embolism Intraductal Papilloma Intravascular Papillary Endothelial Hyperplasia Ischemia Ischemic Colitis Kawasaki Disease Klippel-Feil Syndrome Kommerell Diverticulum Large Cell Carcinoma Laryngitis Late-Onset Focal Dermal Elastosis Lathyrism Leiomyosarcoma Lentigo Maligna Melanoma Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukotriene C4 Synthase Deficiency Limb Ischemia Liposarcoma Lissencephaly 1 Listeriosis Localized Scleroderma Loeys-Dietz Syndrome Loeys-Dietz Syndrome 2 Loeys-Dietz Syndrome 3 Lung Cancer Lung Disease Lung Giant Cell Carcinoma Lupus Erythematosus Lymphoma Magic Syndrome Malignant Renovascular Hypertension Marfan Syndrome Mediastinitis Melanoma Melioidosis Meningocele Metaphyseal Anadysplasia Microcystic Meningioma Microscopic Polyangiitis Mid-Dermal Elastolysis Miliary Tuberculosis Mitral Valve Disease Mixed Gonadal Dysgenesis Mohr-Tranebjaerg Syndrome Mucopolysaccharidosis, Type Vii Myasthenia Gravis Myd88 Deficiency Myocardial Infarction Nasal Cavity Squamous Cell Carcinoma Neonatal Lupus Erythematosus Neuropathy Non-Functioning Paraganglioma Obsessive-Compulsive Disorder Obstructive Jaundice Ocular Motor Apraxia Oral Submucous Fibrosis Orchitis Orofacial Cleft Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteomyelitis Pancreatitis Paraganglioma Paraplegia Paratyphoid Fever Pasteurella Multocida Infection Patent Foramen Ovale Pelvic Organ Prolapse Peptic Ulcer Disease Perianal Hematoma Pericardial Effusion Pericarditis Periodontal Disease Periodontitis Peripheral Artery Disease Peritonitis Phace Syndrome Phacogenic Glaucoma Phaeochromocytoma Pharyngitis Pheochromocytoma Pituitary Adenoma 1, Multiple Types Pleural Empyema Pneumonia Pneumothorax Poliomyelitis Polycystic Kidney Disease Porencephaly Portal Hypertension Proctitis Pseudoxanthoma Elasticum Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis Pulmonary Edema Pulmonary Embolism Pulmonary Emphysema Pulmonary Sequestration Pulmonary Vein Stenosis Pulmonic Stenosis Pyoderma Pyoderma Gangrenosum Q Fever Relapsing Polychondritis Relapsing-Remitting Multiple Sclerosis Renovascular Hypertension Retroperitoneal Fibrosis Retroperitoneal Liposarcoma Rheumatoid Arthritis Right Aortic Arch Ring Chromosome 2 Salmonellosis Sarcoidosis 2 Sciatic Neuropathy Senile Ectropion Severe Hemophilia B Situs Inversus Sorsby Fundus Dystrophy Spastic Ataxia, Charlevoix-Saguenay Type Spastic Entropion Spasticity Spastic Paraparesis Spinal Cord Infarction Spinal Cord Injury Splenomegaly Split-Hand/foot Malformation 1 Spondylitis Spondylolysis Spondyloocular Syndrome Squamous Cell Carcinoma Subclavian Artery Aneurysm Substernal Goiter Superior Mesenteric Artery Syndrome Supravalvular Aortic Stenosis Syphilis Systemic Lupus Erythematosus Takayasu Arteritis Temporal Arteritis Tendinosis Tertiary Syphilis Tetralogy of Fallot Thrombocytopenia Thrombosis Thyroiditis Tolosa-Hunt Syndrome Tracheoesophageal Fistula Transient Global Amnesia Transient Hypogammaglobulinemia of Infancy Transitional Cell Carcinoma Transposition of the Great Arteries Transverse Myelitis Tricuspid Valve Prolapse Tuberous Sclerosis Turner Syndrome Ulcerative Colitis Ureteral Obstruction Urofacial Syndrome 1 Uvula, Bifid Van Der Woude Syndrome 1 Varicose Veins Vascular Disease Wiskott-Aldrich Syndrome Xanthogranulomatous Cholecystitis Xanthomatosis