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 Syndrome métamérique artérioveineux spinal Syndrome de Sturge-Weber Hémangiome infantile de localisation rare Hémangiome congénital rapidement involutif Tumeur vasculaire rare Syndrome de Parkes Weber Syndrome de Maffucci Malformation neurovasculaire Phacomatose cesiomarmorata Fistule artérioveineuse congénitale Angiomatose cutanée et digestive Lymphoedème syndromique Syndrome métamérique artério-veineux cérébro-facial type 3 Malformation veineuse rare Anomalie vasculaire ou angiome Phacomatose cesioflammea Syndrome de microcéphalie-lymphoedème-choriorétinopathie Hygrome kystique Lymphangiectasie intestinale secondaire Lymphangiectasie intestinale primitive Cavernomatose cérébrale familiale Syndrome de surdité-lymphoedème-leucémie Malformation artérioveineuse du maxillaire Phacomatose spilorosea Syndrome PEHO-like Lymphoedème Syndrome LUMBAR Syndrome de Foix-Alajouanine Cutis marmorata telangiectatica congenita Syndrome de dysplasie ectodermique anhidrotique-déficit immunitaire-ostéopétrose-lymphoedème Syndrome de Hennekam Malformation neurocutanée héréditaire Syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique Hémangioendothéliome épithélioïde Malformation artérioveineuse frontonasale Maladie de von Hippel-Lindau Angioma serpiginosum Angiome en touffes Syndrome d'hypotrichose-lymphoedème-télangiectasie-atteinte rénale Malformation veineuse osseuse primaire