{"orpha":79380,"name":"Mixed dermis 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-79380/","orphanet_url":"https://www.orpha.net/en/disease/detail/79380","names":{"fr":{"name":"Anomalie mixte du derme"},"de":{"name":"Hautkrankheit, gemischte Form"},"es":{"name":"Enfermedad mixta de la dermis"},"it":{"name":"Malattia cutanea mista"},"nl":{"name":"Gemengde huidafwijking"},"pt":{"name":"Doença dérmica, mista"},"pl":{"name":"Mieszane zaburzenie skóry właściwej"},"cs":{"name":"Smíšené poruchy dermis"},"uk":{"name":"Змішане захворювання дерми"},"zh":{"name":"混合性真皮疾病"},"tr":{"name":"Karma dermis bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0019294","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19294","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681484","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":974,"name":"Adams-Oliver syndrome","type":"Malformation syndrome"},{"orpha":1114,"name":"Aplasia cutis congenita","type":"Malformation syndrome"},{"orpha":1116,"name":"Aplasia cutis congenita-intestinal lymphangiectasia syndrome","type":"Disease"},{"orpha":1117,"name":"Aplasia cutis-myopia syndrome","type":"Disease"},{"orpha":2092,"name":"Focal dermal hypoplasia","type":"Malformation syndrome"},{"orpha":2556,"name":"Microphthalmia with linear skin defects syndrome","type":"Malformation syndrome"},{"orpha":1214,"name":"Progressive hemifacial atrophy","type":"Disease"},{"orpha":1003,"name":"Scalp defects-postaxial polydactyly syndrome","type":"Malformation syndrome"},{"orpha":2036,"name":"Scalp-ear-nipple syndrome","type":"Malformation syndrome"},{"orpha":805,"name":"Tuberous sclerosis complex","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}