Informaţii despre

Nume Papilledema
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Papilloedema, unspecified
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale

Vezi şi

Boli A-Z Abducens Nerve Disease Abducens Palsy Ablepharon-Macrostomia Syndrome Achondroplasia Acquired Immunodeficiency Syndrome Acromegaly Acute Monoblastic Leukemia Adenoid Hypertrophy Adenoiditis Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aneurysm Angioedema Aniridia 1 Anorexia Nervosa 1 Anosmia Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Antithrombin Iii Deficiency Aplastic Anemia Arachnoid Cysts Arachnoiditis Arteries, Anomalies of Arteriovenous Fistula Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Astrocytoma Barrett's Adenocarcinoma Basal Cell Carcinoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I 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 Brain Small Vessel Disease with or Without Ocular Anomalies Branch Retinal Artery Occlusion Brittle Bone Disorder Brucellosis Budd-Chiari Syndrome Buerger Disease Burkitt Lymphoma Camurati-Engelmann Disease Capillary Hemangioma Carotid Artery Disease Carpal Tunnel Syndrome Castleman Disease Cataract Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Cerebritis Cervicitis Cholecystitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chronic Inflammatory Demyelinating Polyneuropathy Cinca Syndrome Cold Urticaria Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Craniofacial-Deafness-Hand Syndrome Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis Cryopyrin-Associated Periodic Syndrome Cryptococcal Meningitis Cysticercosis Cystinosis Demyelinating Polyneuropathy Developmental Dysplasia of the Hip 1 Encephalitis Encephalopathy Endemic Typhus Ependymoma Epidermoid Brain Cyst Epidermoid Cysts Esotropia Familial Cold Autoinflammatory Syndrome Familial Cold Autoinflammatory Syndrome 1 Foster-Kennedy Syndrome Granulomatous Angiitis Guillain-Barre Syndrome Headache Head Injury Hemangioma Hemoglobinuria Hepatic Infarction Histiocytosis Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hypervitaminosis a Hypoparathyroidism Hypothalamic Hamartomas Infective Endocarditis Intermittent Claudication Intracranial Hypertension Intracranial Hypertension, Idiopathic Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Leukemia Livedoid Vasculopathy Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Malaria Malignant Hypertension Mantle Cell Lymphoma Melanoma Meningitis Miller Fisher Syndrome Muckle-Wells Syndrome Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis Type Vi Muscular Dystrophy Myhre Syndrome Myxedema Neurilemmoma Neuritis Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neurosarcoidosis Nipples, Supernumerary Obstructive Hydrocephalus Optic Disk Drusen Optic Neuritis Optic Papillitis Otitis Externa Paraganglioma Paraneoplastic Syndromes Paroxysmal Nocturnal Hemoglobinuria Peripheral Vertigo Pfeiffer Syndrome Pilocytic Astrocytoma Pituitary Tumors Placental Abruption Plasmacytoma Poems Syndrome Poliomyelitis Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polyneuropathy Polyradiculoneuropathy Portal Vein Thrombosis Prostate Disease Prostatitis Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudopapilledema Pulmonary Embolism Pulmonary Emphysema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pycnodysostosis Pyoderma Radiculopathy Raynaud Disease Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Rickets Rosai-Dorfman Disease Sagittal Sinus Thrombosis Schnitzler Syndrome Sleep Apnea Sneddon Syndrome Spinal Cancer Spinal Cord Infarction Splenic Infarction Squamous Cell Papilloma Streptococcal Meningitis Syphilitic Meningitis Syringomyelia Systemic Lupus Erythematosus Thrombocytosis Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Tonsillitis Transient Erythroblastopenia of Childhood Tuberous Sclerosis Turner Syndrome Uveitis Vascular Disease Vulvar Vestibulitis Syndrome Wrinkles Xeroderma Pigmentosum, Variant Type