SE-ATLAS

17q11 microdeletion syndrome Angioma serpiginosum Angioosteohypertrophic syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Aplasia cutis congenita-intestinal lymphangiectasia syndrome Blue rubber bleb nevus Bockenheimer syndrome CLAPO syndrome CLOVES syndrome Capillary malformation-arteriovenous malformation Cavernous hemangiomas of face-supraumbilical midline raphe syndrome Cerebral arteriovenous malformation Cerebrofacial arteriovenous metameric syndrome Cerebrofacial arteriovenous metameric syndrome type 1 Cerebrofacial arteriovenous metameric syndrome type 3 Cholestasis-lymphedema syndrome Complex vascular malformation with associated anomalies Congenital arteriovenous fistula Congenital systemic arteriovenous fistula Cutis marmorata telangiectatica congenita Cystic hygroma Dahlberg-Borer-Newcomer syndrome Dandy-Walker malformation-facial hemangioma syndrome Deafness-lymphedema-leukemia syndrome Diffuse lymphatic malformation Diffuse neonatal hemangiomatosis Dural sinus malformation Epithelioid hemangioendothelioma Facial arteriovenous malformation Familial cerebral cavernous malformation Familial multiple nevi flammei Foix-Alajouanine syndrome Frontonasal arteriovenous malformation German syndrome Glomuvenous malformation Hemihyperplasia-multiple lipomatosis syndrome Hennekam syndrome Hereditary hemorrhagic telangiectasia Hereditary neurocutaneous malformation Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Infantile hemangioma of rare localization Internal carotid absence Intestinal lymphangiectasia Inverse Klippel-Trénaunay syndrome Kaposiform hemangioendothelioma Kasabach-Merritt phenomenon Klippel-Trénaunay syndrome LUMBAR syndrome Laryngotracheal angioma Lipedema Lymphedema Lymphedema-atrial septal defects-facial changes syndrome Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome Lymphedema-distichiasis syndrome Macrocystic lymphatic malformation Maffucci syndrome Mandibular arteriovenous malformation Maxillary arteriovenous malformation Megalencephaly-capillary malformation-polymicrogyria syndrome Microcephaly-lymphedema-chorioretinopathy syndrome Microcystic lymphatic malformation Mucocutaneous venous malformations Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Neurovascular malformation Non-involuting congenital hemangioma PEHO-like syndrome PHACE syndrome Parkes Weber syndrome Phakomatosis cesioflammea Phakomatosis cesiomarmorata Phakomatosis pigmentovascularis Phakomatosis spilorosea Primary intestinal lymphangiectasia Primary intraosseous venous malformation Primary lymphedema Proteus syndrome Pulmonary arteriovenous malformation Rapidly involuting congenital hemangioma Rare arteriovenous malformation Rare capillary malformation Rare circulatory system disease Rare lymphatic malformation Rare lymphatic system anomaly Rare vascular tumor Rare venous malformation Retinal capillary malformation Secondary intestinal lymphangiectasia Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Simple vascular malformation Spinal arteriovenous metameric syndrome Spindle cell hemangioma Sternal malformation-vascular dysplasia syndrome Sturge-Weber syndrome Syndromic lymphedema Transverse limb deficiency-hemangioma syndrome Tufted angioma Vascular anomaly or angioma Vein of Galen aneurysmal malformation Von Hippel-Lindau disease Wyburn-Mason syndrome Yellow nail syndrome