Informaţii despre

Nume Klippel-Trenaunay-Weber Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation syndromes predominantly involving limbs
Clasificare anatomică Malacards Boli cardiovasculare; Boli de piele; Boli osoase

Vezi şi

Boli A-Z Adie Pupil Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm Angiodysplasia Angiokeratoma Angiokeratoma Circumscriptum Angiomatosis Angiomyomatous Hamartoma Angioosteohypertrophic Syndrome Aniridia 1 Anorexia Nervosa 1 Antithrombin Iii Deficiency Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Basal Cell Carcinoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Capillary Hemangioma Capillary Malformations, Congenital Carotid Artery Occlusion Cataract Cavernous Hemangioma Cavernous Lymphangioma Cavernous Malformation Cell Type Benign Neoplasm Central Nervous System Hemangioma Cerebral Cavernous Malformations Cerebral Cavernous Malformations 2 Cerebral Cavernous Malformations 3 Cerebritis Cervicitis Chronic Ulcer of Skin Chylothorax, Congenital Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Lymphedema Congenital Nystagmus Congestive Heart Failure Cranio-Facial Dystonia Cryptorchidism, Unilateral or Bilateral Disseminated Intravascular Coagulation Double Inferior Vena Cava Duodenitis Epidural Neoplasm Factor Vii Deficiency Fallopian Tube Carcinoma Fanconi Anemia, Complementation Group E Gestational Trophoblastic Neoplasm Giant Hemangioma Gigantism Gingivitis Glioblastoma Glioblastoma Multiforme Glioma Glomuvenous Malformations Gorham's Disease Hantavirus Pulmonary Syndrome Hemangioma Hemihyperplasia, Isolated Hemimegalencephaly Hepatic Adenomas, Familial Hereditary Lymphedema Human Venous Malformation Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypospadias Intracranial Aneurysm Leiomyoma Lower Limb Hypertrophy Lymphangioma Lymphatic Malformations Lymphedema Lymphedema, Hereditary, Ii Major Affective Disorder 8 Major Affective Disorder 9 May-Thurner Syndrome Mediastinitis Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome Melorheostosis Meningitis Metatypical Basal Cell Carcinoma Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Osteoblastoma Paraplegia Parkes Weber Syndrome Parkinson Disease, Late-Onset Patent Foramen Ovale Peripartum Cardiomyopathy Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Phacomatosis Pigmentovascularis Pik3ca-Related Overgrowth Spectrum Polydactyly Polykaryocytosis Inducer Proteus Syndrome Pulmonary Embolism Pyoderma Pyoderma Gangrenosum Retinitis Ring Chromosome 18 Sacrococcygeal Teratoma Sarcoma Scoliosis Sensorineural Hearing Loss Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Splenomegaly Squamous Cell Carcinoma Sturge-Weber Syndrome Teratoma Thrombophilia Thrombosis Trophoblastic Neoplasm Tungiasis Urethritis Vaginal Discharge Vaginitis Varicose Veins Vascular Disease Vascular Hemostatic Disease Venous Malformations, Multiple Cutaneous and Mucosal Weber Syndrome Wilms Tumor 6 Yellow Nail Syndrome