{"orpha":717868,"name":"Rare skin disease with inflammatory bowel 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-717868/","orphanet_url":"https://www.orpha.net/en/disease/detail/717868","names":{"fr":{"name":"Maladie rare de la peau avec maladie inflammatoire de l'intestin"},"de":{"name":"Seltene Hautkrankheit mit entzündlicher Darmerkrankung"},"es":{"name":"Enfermedad cutánea rara con enfermedad inflamatoria intestinal"},"it":{"name":"Malattia cutanea rara con malattia infiammatoria dell'intestino"},"nl":{"name":"Zeldzame huidziekte met inflammatoire darmziekte"},"pt":{"name":"Rare skin disease with inflammatory bowel disease"},"pl":{"name":"Rare skin disease with inflammatory bowel disease"},"cs":{"name":"Rare skin disease with inflammatory bowel disease"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":717862,"name":"Rare disorder with inflammatory bowel disease","classifications":[152,156,233]}],"children":[{"orpha":303,"name":"Dystrophic epidermolysis bullosa","type":"Clinical group"},{"orpha":464,"name":"Incontinentia pigmenti","type":"Malformation syndrome"},{"orpha":2908,"name":"Kindler epidermolysis bullosa","type":"Disease"},{"orpha":85453,"name":"X-linked reticulate pigmentary disorder","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}