{"orpha":2051,"name":"Fraser-like 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 Fraser syndrome","url":"https://raremap.alftech.space/d/ORPHA-2051/","orphanet_url":"https://www.orpha.net/en/disease/detail/2051","names":{"fr":{"name":"Syndrome Fraser-like"},"de":{"name":"Fraser-ähnliches Syndrom"},"es":{"name":"Síndrome similar a Fraser","synonyms":["Síndrome de Fraser-like"]},"it":{"name":"Sindrome Fraser-simile"},"nl":{"name":"Fraser-achtig syndroom"},"pt":{"name":"Síndrome Fraser-<i>like"},"pl":{"name":"Zespół podobny do zespołu Frasera"},"cs":{"name":"Syndrom podobný Fraserovu"},"uk":{"name":"Синдром Фрейзер-подібний"},"zh":{"name":"类弗雷泽综合征,类隐眼畸形"},"tr":{"name":"Fraser benzeri sendrom"}},"xrefs":[{"source":"OMIM","code":"229230","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1856708","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":2052,"name":"Fraser syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}