{"orpha":228272,"name":"Primary anetoderma","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":["Primary macular atrophy"],"definition":"Primary anetoderma is a rare skin disease characterized by loss of elastin tissue resulting in localized areas of flaccid skin in the absence of a secondary cause.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-228272/","orphanet_url":"https://www.orpha.net/en/disease/detail/228272","names":{"fr":{"name":"Anétodermie primitive","synonyms":["Atrophie maculaire primitive"],"definition":"Maladie rare de la peau caractérisée par une perte de tissu élastique entraînant des zones localisées de relâchement de la peau en l'absence de cause secondaire."},"de":{"name":"Anetodermie, primäre","synonyms":["Makulaatrophie, primäre"]},"es":{"name":"Anetodermia primaria","synonyms":["Atrofia macular primaria"],"definition":"Es una enfermedad cutánea poco frecuente caracterizada por la pérdida de tejido elastico dérmico en ausencia de una causa subyacente, ocasionando áreas localizadas de piel flácida."},"it":{"name":"Anetoderma primitivo","synonyms":["Atrofia maculare primitiva"],"definition":"L'anetoderma primitivo è una malattia cutanea rara, caratterizzata dalla perdita di tessuto elastico, che esita nella formazione di aree localizzate di cute flaccida; la causa della malattia non è nota."},"nl":{"name":"Primaire anetodermie","synonyms":["Primaire macula-atrofie"],"definition":"Primaire anetodermie is een zeldzame huidziekte die gekarakteriseerd wordt door verlies van elastineweefsel, wat leidt tot gelokaliseerde gebieden met slappe huid, in afwezigheid van een secundaire oorzaak."},"pt":{"name":"Anetoderma primário"},"pl":{"name":"Pierwotny zanik skórny plackowaty","synonyms":["Pierwotny zanik plamki"]},"cs":{"name":"Primární anetodermie","synonyms":["Primární makulární atrofie"]},"uk":{"name":"Первинна анетодермія","synonyms":["Первинна макулярна атрофія"],"definition":"Primary anetoderma is a rare skin disease characterized by loss of elastin tissue resulting in localized areas of flaccid skin in the absence of a secondary cause."},"zh":{"name":"原发性皮肤松垂","synonyms":["原发性斑状萎缩"],"definition":"原发性皮肤松垂是一种罕见的皮肤病，其特征是在没有继发原因的情况下弹性蛋白组织缺失，导致局部皮肤松弛。"},"tr":{"name":"Primer anetoderma","synonyms":["Primer maküler atrofi"]}},"xrefs":[{"source":"ICD-10","code":"L90.1","qualifier":"BTNT","icd_relation":"specific","validated":true},{"source":"ICD-10","code":"L90.2","qualifier":"BTNT","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"EE41.1","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"308286033"},{"source":"MONDO","code":"0016444","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D057088","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0406550","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":89826,"name":"Rare skin disease"},"parents":[{"orpha":228221,"name":"Acquired dermis elastic tissue disorder with decreased elastic tissue","classifications":[187]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["All ages"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}