SE-ATLAS

Cutis marmorata telangiectatica congenita CLAPO syndrome Blue rubber bleb nevus Mixed cystic lymphatic malformation Vein of Galen aneurysmal malformation Dural sinus malformation Facial arteriovenous malformation Gorham-Stout disease Diffuse neonatal hemangiomatosis Meige disease Milroy disease Inverse Klippel-Trénaunay syndrome Phakomatosis cesioflammea Phakomatosis spilorosea Phakomatosis cesiomarmorata Microcystic lymphatic malformation Sturge-Weber syndrome Megalencephaly-capillary malformation-polymicrogyria syndrome CLOVES syndrome Primary laryngeal lymphangioma Klippel-Trénaunay syndrome Lymphedema-distichiasis syndrome Hereditary hemorrhagic telangiectasia Angioosteohypertrophic syndrome Maffucci syndrome Proteus syndrome Primary intestinal lymphangiectasia Phakomatosis pigmentovascularis Hemihyperplasia-multiple lipomatosis syndrome Rare arteriovenous malformation Lymphedema-posterior choanal atresia syndrome Rare lymphatic malformation Maxillary arteriovenous malformation Frontonasal arteriovenous malformation Mandibular arteriovenous malformation Familial cerebral cavernous malformation Cholestasis-lymphedema syndrome Macrocystic lymphatic malformation Rare venous malformation Cerebrofacial arteriovenous metameric syndrome Cerebrofacial arteriovenous metameric syndrome type 1 Cerebrofacial arteriovenous metameric syndrome type 3 Mucocutaneous venous malformations Proteus-like syndrome Overgrowth-macrocephaly-facial dysmorphism syndrome Capillary malformation-arteriovenous malformation Kaposiform lymphangiomatosis Wyburn-Mason syndrome Congenital systemic arteriovenous fistula Primary lymphedema Common cystic lymphatic malformation PIK3CA-related overgrowth syndrome Intestinal lymphangiectasia Spinal arteriovenous metameric syndrome Glomuvenous malformation Cowden syndrome Rare capillary malformation with associated anomalies Rare combined vascular malformation Familial multiple nevi flammei Microcephaly-capillary malformation syndrome Port-wine nevi-mega cisterna magna-hydrocephalus syndrome Primary intraosseous venous malformation Parkes Weber syndrome Angioma serpiginosum Familial cylindromatosis Kasabach-Merritt phenomenon Rare capillary malformation Seltene Fehlbildung des Lymphatischen Systems Komplexe Vaskuläre Fehlbildung mit assoziierten Anomalien Lymphödem-zerebrale arteriovenöse Fehlbildung-primäre pulmonale Hypertonie-Syndrom Segmentaler Auswuchs-Lipomatose-arteriovenöse Fehlbildung-epidermaler Naevus-Syndrom Lymphatische Fehlbildung, diffuse Bockenheimer-Syndrom Verruköses Hämangiom Fehlbildung, arteriovenöse pulmonale