SE-ATLAS

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