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Nume Weber Syndrome
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Boli A-Z Acute Closed-Angle Glaucoma Acute Leukemia Adenoma Aging Al-Raqad Syndrome Aneurysm Angiodysplasia Angioid Streaks Angiomatosis Angiomatous Meningioma Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Arteriovenous Fistula Arteriovenous Malformation Arteriovenous Malformations of the Brain Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autosomal Dominant Polycystic Kidney Disease Basal Cell Carcinoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Blood Group--Swann System Brain Edema Capillary Malformations, Congenital Carpal Tunnel Syndrome Cataract Cavernous Lymphangioma Cavernous Malformation Central Retinal Vein Occlusion Cerebral Atrophy Cerebritis Cervicitis Childhood Leukemia Choroiditis Chronic Ulcer of Skin Coats Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Nystagmus Congenital Short Femur Cryptorchidism, Unilateral or Bilateral Cutis Laxa Cutis Marmorata Telangiectatica Congenita Cystic Disease of Lung Disseminated Intravascular Coagulation Double Inferior Vena Cava Duodenitis Dystonia Early-Onset Glaucoma Encephalitis Encephalopathy Endotheliitis Epidural Neoplasm Epilepsy Esotropia Fabry Disease Fanconi Anemia, Complementation Group E Femoral Agenesis/hypoplasia Fibromatosis Gardner-Diamond Syndrome Gingival Fibromatosis Gingival Overgrowth Gingivitis Glioblastoma Glioblastoma Multiforme Glioma Growth Hormone Deficiency Headache Head Injury Hemangioma Hemimegalencephaly Hemiplegia Hemiplegic Migraine Hepatitis Hereditary Hemorrhagic Telangiectasia Heritable Pulmonary Arterial Hypertension Heterochromia Iridis Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanosis of Ito Hypopituitarism Hypospadias Hypoxia Ischemia Klippel-Trenaunay-Weber Syndrome Leukemia Leukocoria Leukodystrophy, Hypomyelinating, 6 Lower Limb Hypertrophy Lymphangioma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive May-Thurner Syndrome Megalencephaly Melanoma Melorheostosis Mental Retardation Syndrome, Mietens-Weber Type Mongolian Spot Mononeuropathy of the Median Nerve, Mild Myeloma, Multiple Myoclonic Astatic Epilepsy Myopia Nephrotic Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Nevus of Ota Nodular Nonsuppurative Panniculitis Osteoblastoma Pancytopenia Panniculitis Paraplegia Parkes Weber Syndrome Periodontitis Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Phacomatosis Pigmentovascularis Pleomorphic Xanthoastrocytoma Poems Syndrome Polycystic Kidney Disease Posterior Scleritis Proteus Syndrome Psychotic Disorder Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Arteriovenous Malformation Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Primary, 1 Pyoderma Pyoderma Gangrenosum Pyogenic Granuloma Rasmussen Encephalitis Retinal Detachment Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Rubeosis Iridis Sacrococcygeal Teratoma Scleritis Scoliosis Seizure Disorder Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin Hemangioma Sleep Apnea Sporadic Hemiplegic Migraine Status Epilepticus Strabismus Sturge-Weber Syndrome Telangiectasia, Hereditary Hemorrhagic, Type 1 Telangiectasia, Hereditary Hemorrhagic, Type 3 Telangiectasis Teratoma Thrombophilia Thrombosis Thyroiditis Tuberous Sclerosis Urethritis Vaginal Discharge Vaginitis Varicose Veins Vein of Galen Aneurysm Von Hippel-Lindau Syndrome