{"orpha":79379,"name":"Skin vascular disease","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-79379/","orphanet_url":"https://www.orpha.net/en/disease/detail/79379","names":{"fr":{"name":"Maladie vasculaire du derme"},"de":{"name":"Hautkrankheit, vaskuläre"},"es":{"name":"Enfermedad vascular de la piel"},"it":{"name":"Malattia cutanea vascolare"},"nl":{"name":"Huidvasculaire ziekte"},"pt":{"name":"Doença vascular cutânea"},"pl":{"name":"Choroba naczyń skórnych"},"cs":{"name":"Vaskulární onemocnění kůže"},"uk":{"name":"Захворювання судин шкіри"},"zh":{"name":"皮肤血管疾病"},"tr":{"name":"Deri vasküler hastalığı"}},"xrefs":[{"source":"MONDO","code":"0019293","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19293","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D017445","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0162819","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10062171","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":79377,"name":"Dermis disorder","classifications":[187]}],"children":[{"orpha":719936,"name":"Angiokeratoma of Mibelli","type":"Morphological anomaly"},{"orpha":95429,"name":"Angioma serpiginosum","type":"Disease"},{"orpha":100,"name":"Ataxia-telangiectasia","type":"Disease"},{"orpha":251347,"name":"Ataxia-telangiectasia-like disorder","type":"Disease"},{"orpha":656071,"name":"Atrophic papulosis","type":"Disease"},{"orpha":1059,"name":"Blue rubber bleb nevus syndrome","type":"Malformation syndrome"},{"orpha":280065,"name":"Calciphylaxis cutis","type":"Clinical subtype"},{"orpha":90308,"name":"Capillary-lymphatic-venous malformation with segmental distribution","type":"Disease"},{"orpha":90280,"name":"Chilblain lupus","type":"Disease"},{"orpha":280779,"name":"Cutaneous collagenous vasculopathy","type":"Disease"},{"orpha":1556,"name":"Cutis marmorata telangiectatica congenita","type":"Malformation syndrome"},{"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":280774,"name":"Generalized essential telangiectasia","type":"Disease"},{"orpha":774,"name":"Hereditary hemorrhagic telangiectasia","type":"Disease"},{"orpha":542643,"name":"Livedoid vasculopathy","type":"Clinical syndrome"},{"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"},{"orpha":529864,"name":"Secondary erythromelalgia","type":"Disease"},{"orpha":217008,"name":"Segmental venous malformation","type":"Malformation syndrome"},{"orpha":53721,"name":"Spinal arteriovenous metameric syndrome","type":"Malformation syndrome"},{"orpha":3205,"name":"Sturge-Weber syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}