{"orpha":3087,"name":"Retinohepatoendocrinologic syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Alström syndrome","url":"https://raremap.alftech.space/d/ORPHA-3087/","orphanet_url":"https://www.orpha.net/en/disease/detail/3087","names":{"fr":{"name":"Syndrome rétino-hépato-endocrinologique"},"de":{"name":"Retino-hepato-endokrinologisches Syndrom","synonyms":["Hansen-Larsen-Berg-Syndrom"]},"es":{"name":"Retino hepato endocrinológico síndrome"},"it":{"name":"Sindrome retino-epato-endocrinologica"},"nl":{"name":"Retinohepato-endocrinologisch syndroom"},"pt":{"name":"Síndrome retino-hepato-endocrinológico"},"pl":{"name":"Zespół siatkówkowo-wątrobowo-endokrynologiczny"},"cs":{"name":"Retinohepatoendokrinologický syndrom"},"uk":{"name":"Ретиногепатоендокринологічний синдром"},"zh":{"name":"视网膜-肝-内分泌综合征"},"tr":{"name":"Retinohepatoendokrinolojik sendrom"}},"xrefs":[{"source":"OMIM","code":"268040","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1849399","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"4685","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":64,"name":"Alström syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}