{"orpha":103915,"name":"OBSOLETE: Immunoproliferative small intestinal disease","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: IPSID","OBSOLETE: Mediterranean lymphoma"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Alpha-heavy chain disease","url":"https://raremap.alftech.space/d/ORPHA-103915/","orphanet_url":"https://www.orpha.net/en/disease/detail/103915","names":{"fr":{"name":"OBSOLETE : Maladie immunoproliférative de l'intestin grle","synonyms":["OBSOLETE : IPSID","OBSOLETE : Lymphome méditerranéen"]},"de":{"name":"OBSOLET: Immunproliferative Dünndarmkrankheit","synonyms":["OBSOLET: IPSID","OBSOLET: Mediterranes Lymphom"]},"es":{"name":"OBSOLETO: Enfermedad inmunoproliferativa del intestino delgado","synonyms":["OBSOLETO: EIPID","OBSOLETO: Linfoma mediterráneo"]},"it":{"name":"OBSOLETO: Malattia immunoproliferativa dell'intestino tenue","synonyms":["OBSOLETO: Linfoma mediterraneo","OBSOLETO: IPSID"]},"nl":{"name":"OBSOLEET: Immunoproliferatieve dunne darmziekte","synonyms":["OBSOLEET: IPSID","OBSOLEET: Mediterraan lymfoom"]},"pt":{"name":"OBSOLETO: Doença imunoproliferativa do intestino delgado"},"pl":{"name":"NIEAKTUALNE: Immunoproliferacyjna choroba jelita cienkiego","synonyms":["NIEAKTUALNE: Chłoniak śródziemnomorski","NIEAKTUALNE: IPSID"]},"cs":{"name":"NEAKTUÁLNÍ: Imunoproliferativní onemocnění tenkého střeva","synonyms":["OBSOLETE: IPSID","OBSOLETE: Mediterranean lymphoma"]},"uk":{"name":"ЗАСТАРІЛО: Імунопроліферативне захворювання тонкої кишки","synonyms":["ЗАСТАРІЛО: IPSID","ЗАСТАРІЛО: Середземноморська лімфома"]},"zh":{"name":"弃用：免疫增生性小肠疾病","synonyms":["地中海淋巴瘤"]},"tr":{"name":"Eski adı: İmmünoproliferatif ince bağırsak hastalığı","synonyms":["IPSID","Akdeniz lenfoması"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":100025,"name":"Alpha-heavy chain disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}