{"orpha":183478,"name":"Genetic skin vascular disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-183478/","orphanet_url":"https://www.orpha.net/en/disease/detail/183478","names":{"fr":{"name":"Anomalie vasculaire cutanée génétique"},"de":{"name":"Hautkrankheit, vaskuläre, genetisch bedingte"},"es":{"name":"Enfermedad vascular cutánea genética"},"it":{"name":"Malattia vascolare cutanea genetica"},"nl":{"name":"Genetische vasculaire huidaandoening"},"pt":{"name":"Doença dermatológica vascular, genética"},"pl":{"name":"Genetic skin vascular disorder"},"cs":{"name":"Geneticky podmíněné poruchy kožních cév"},"uk":{"name":"Генетично обумовлене захворювання судин шкіри"},"zh":{"name":"遗传性皮肤血管异常"},"tr":{"name":"Genetik deri vasküler bozukluğu"}},"xrefs":[{"source":"MONDO","code":"15948","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680572","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":183472,"name":"Genetic dermis disorder","classifications":[156]}],"children":[{"orpha":95429,"name":"Angioma serpiginosum","type":"Disease"},{"orpha":100,"name":"Ataxia-telangiectasia","type":"Disease"},{"orpha":656071,"name":"Atrophic papulosis","type":"Disease"},{"orpha":1059,"name":"Blue rubber bleb nevus syndrome","type":"Malformation syndrome"},{"orpha":90308,"name":"Capillary-lymphatic-venous malformation with segmental distribution","type":"Disease"},{"orpha":90280,"name":"Chilblain lupus","type":"Disease"},{"orpha":324,"name":"Fabry disease","type":"Disease"},{"orpha":481662,"name":"Familial Chilblain lupus","type":"Disease"},{"orpha":313846,"name":"Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome","type":"Disease"},{"orpha":624,"name":"Familial multiple nevi flammei","type":"Morphological anomaly"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":163634,"name":"Maffucci syndrome","type":"Disease"},{"orpha":60040,"name":"Megalencephaly-capillary malformation-polymicrogyria syndrome","type":"Malformation syndrome"},{"orpha":90307,"name":"Parkes Weber syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}