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To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-717757/","orphanet_url":"https://www.orpha.net/en/disease/detail/717757","names":{"fr":{"name":"Maladie immunologique rare associée à une maladie inflammatoire de l'intestin"},"de":{"name":"Seltene Immunkrankheit mit entzündlicher Darmerkrankung"},"es":{"name":"Enfermedad inmunológica rara con enfermedad inflamatoria intestinal"},"it":{"name":"Malattia immunitaria rara con malattia infiammatoria dell'intestino"},"nl":{"name":"Zeldzame immuunziekte met inflammatoire darmziekte"},"pt":{"name":"Rare immune disease with inflammatory bowel disease"},"pl":{"name":"Rare immune disease with inflammatory bowel disease"},"cs":{"name":"Rare immune disease with inflammatory bowel disease"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":717862,"name":"Rare 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syndrome","type":"Disease"},{"orpha":695183,"name":"Late-onset combined immunodeficiency due to ICOS deficiency","type":"Disease"},{"orpha":99842,"name":"Leukocyte adhesion deficiency type I","type":"Clinical subtype"},{"orpha":294023,"name":"Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome","type":"Disease"},{"orpha":229717,"name":"Non-syndromic agammaglobulinemia","type":"Disease"},{"orpha":39041,"name":"Omenn syndrome","type":"Disease"},{"orpha":596759,"name":"RELA haploinsufficiency-associated inflammatory disease","type":"Disease"},{"orpha":391487,"name":"STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome","type":"Disease"},{"orpha":438159,"name":"STAT3-related early-onset multisystem autoimmune disease","type":"Disease"},{"orpha":331176,"name":"Severe congenital neutropenia due to G6PC3 deficiency","type":"Disease"},{"orpha":445018,"name":"Syndromic autoimmune enteropathy due to LRBA 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