Informaţii despre

Nume Arteriovenous Malformation
Pagina Web www.malacards.org
Clasificare globală Malacards Bolile canceroase
Clasificari ICD10 Arteriovenous fistula, acquired

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Acute Pancreatitis Acute Respiratory Distress Syndrome Acute Transverse Myelitis Adamantinous Craniopharyngioma Adenoma Adult Astrocytic Tumour Aging Alexia Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amphetamine Abuse Anaplastic Oligodendroglioma Aneurysm Angina Pectoris Angiodysplasia Angiokeratoma Circumscriptum Angiomatosis Angioma, Tufted Aniridia 1 Anorexia Nervosa 1 Aplasia Cutis Congenita Arteriovenous Fistula Arteriovenous Malformations of the Brain Arthritis Arthrochalasia Ehlers-Danlos Syndrome Astroblastoma Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atypical Autism Autism Azoospermia Back Pain Bannayan-Riley-Ruvalcaba Syndrome Basal Ganglia Calcification Basilar Artery Occlusion Beckwith-Wiedemann Syndrome Benign Metastasizing Leiomyoma Birt-Hogg-Dube Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharochalasis Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Cancer Brain Edema Branch Retinal Artery Occlusion Breast Cancer Capillary Hemangioma Capillary Malformation-Arteriovenous Malformation Capillary Malformations, Congenital Cauda Equina Syndrome Cavernous Hemangioma Cavernous Malformation Central Nervous System Vasculitis Central Retinal Vein Occlusion Cerebral Aneurysms Cerebral Cavernous Malformations Cerebral Hemorrhage Cerebral Palsy Cerebritis Cerebrovascular Disease Cervicitis Chiari Malformation Chiari Malformation Type I Chiasmal Syndrome Choroiditis Chronic Hiccups Chronic Thromboembolic Pulmonary Hypertension Cobb Syndrome Colitis Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congestive Heart Failure Connective Tissue Disease Constrictive Pericarditis Corneal Ulcer Cowden Disease Cowden Syndrome 1 Craniosynostosis 1 Critical Limb Ischemia Crouzon Syndrome with Acanthosis Nigricans Cutaneous Mastocytosis Cyanosis, Transient Neonatal Cystitis Diabetic Foot Ulcers Diffuse Lymphatic Malformation Disseminated Intravascular Coagulation Duodenal Ulcer Duodenitis Dyskeratosis Congenita Dysphagia Encephalocele Endotheliitis Exophthalmos Extra-Adrenal Pheochromocytoma Extracranial Arteriovenous Malformation Facial Arteriovenous Malformation Facial Paralysis Factor V Deficiency Familial Adenomatous Polyposis Fanconi Anemia, Complementation Group E Fasciitis Foix-Alajouanine Syndrome Ganglioneuroma Gastrointestinal Stromal Tumor Gestational Trophoblastic Tumor Giant Cell Tumor Gingival Hypertrophy Gingivitis Glioblastoma Glioblastoma Multiforme Glioma Glomeruloid Hemangioma Glossopharyngeal Neuralgia Headache Hemangioblastoma Hemangioendothelioma Hemangioma Hemarthrosis Hemifacial Spasm Hemifacial Spasm, Familial Hemiplegic Migraine Hemophilia Hemophilia a Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hepatitis Hepatopulmonary Syndrome Hereditary Hemorrhagic Telangiectasia Heritable Pulmonary Arterial Hypertension Heterotaxy Heterotaxy, Visceral, 1, X-Linked Human Venous Malformation Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypotrichosis Hypoxia Immune Hydrops Fetalis Inflammatory Bowel Disease Internuclear Ophthalmoplegia Interstitial Nephritis Intracranial Aneurysm Intracranial Embolism Intracranial Hypertension Invasive Mole Ischemia Ischemic Colitis Ischemic Retinopathy Juvenile Pilocytic Astrocytoma Kawasaki Disease Klippel-Trenaunay-Weber Syndrome Leiomyoma Lipomatosis Lipomyelomeningocele Liver Cirrhosis Lung Cancer Lymphangioma Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Malignant Glioma Mandibular Arteriovenous Malformation Maxillary Arteriovenous Malformation Mccune-Albright Syndrome Medial Medullary Syndrome Median Arcuate Ligament Syndrome Mediastinitis Medulloblastoma Meningioma, Familial Meningitis Meningothelial Meningioma Migraine with Aura Mixed Connective Tissue Disease Moyamoya Disease 1 Mucinous Stomach Adenocarcinoma Mucositis Mutism Myocardial Infarction Myoclonus Myoma Nasopharyngitis Necrotizing Fasciitis Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuromyelitis Optica Neuronitis Neuropathy Nevus of Ota Obstructive Hydrocephalus Oligodendroglioma Orbital Lymphangioma Osteomyelitis Pancreatitis Papilledema Paraplegia Parkes Weber Syndrome Patent Ductus Venosus Patent Foramen Ovale Pericardial Effusion Pericarditis Peritonitis Petrositis Phace Syndrome Pheochromocytoma Pilocytic Astrocytoma Pituitary Adenoma Pleomorphic Xanthoastrocytoma Plexiform Neurofibroma Pneumonia Pneumothorax Poems Syndrome Polycystic Kidney Disease Polycythemia Polycythemia Vera Preauricular Sinus Prosopagnosia Protein S Deficiency Proteus-Like Syndrome Proteus Syndrome Pseudoxanthoma Elasticum Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Arteriovenous Malformation Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Hypertension, Primary, 1 Pulmonary Sequestration Pulmonary Venoocclusive Disease Pyogenic Granuloma Rapidly Involuting Congenital Hemangioma Recurrent Acute Pancreatitis Renovascular Hypertension Retinal Artery Occlusion Retinal Degeneration Retinitis Rheumatoid Nodulosis Rosacea Ruvalcaba Syndrome Schimmelpenning-Feuerstein-Mims Syndrome Schizencephaly Segmental Outgrowth-Lipomatosis-Arteriovenous Malformation-Epidermal Nevus Syndrome Seizure Disorder Sertoli Cell Tumor Severe Hemophilia a Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sick Building Syndrome Siderosis Skin Epithelioid Hemangioma Skin Hemangioma Sorsby Fundus Dystrophy Spastic Ataxia, Charlevoix-Saguenay Type Spastic Entropion Spasticity Spastic Monoplegia Spinal Cord Infarction Spinal Disease Splenic Artery Aneurysm Splenic Infarction Sporadic Hemiplegic Migraine Squamous Cell Carcinoma, Head and Neck Squamous Cell Carcinoma of the Hypopharynx Sturge-Weber Syndrome Superficial Siderosis Superior Mesenteric Artery Syndrome Sveinsson Chorioretinal Atrophy Swyer-James Syndrome Syncope Syringomyelia Takayasu Arteritis Telangiectasia, Hereditary Hemorrhagic, Type 1 Telangiectasia, Hereditary Hemorrhagic, Type 2 Telangiectasis Teratoma Thrombocytopenia Thrombophlebitis Thrombosis Thyroiditis Tic Disorder Trigeminal Neuralgia Turner Syndrome Twin-to-Twin Transfusion Syndrome Ureteral Obstruction Ureterocele Vaginitis Varicocele Varicose Veins Vasculitis Vein of Galen Aneurysm Venous Malformations, Multiple Cutaneous and Mucosal Weber Syndrome Wyburn Mason's Syndrome