{"orpha":99777,"name":"Achalasia-alacrimia syndrome","type":"Disease","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 Triple A syndrome","url":"https://raremap.alftech.space/d/ORPHA-99777/","orphanet_url":"https://www.orpha.net/en/disease/detail/99777","names":{"fr":{"name":"Syndrome d'achalasie-alacrymie"},"de":{"name":"Achalasie-Alakrimie-Syndrom"},"es":{"name":"Síndrome de acalasia alacrimia"},"it":{"name":"Sindrome acalasia-alacrimia"},"nl":{"name":"Achalasie-alacrimiesyndroom"},"pt":{"name":"Síndrome acalasia-alacrimia"},"pl":{"name":"Zespół achalazja-alakrimia"},"cs":{"name":"Syndrom zahrnující achalazii a alakrimii"},"uk":{"name":"Синдром ахалазії-алакримії"},"zh":{"name":"贲门失弛缓-无泪综合征"},"tr":{"name":"Akalazya-alakimia sendromu"}},"xrefs":[{"source":"MeSH","code":"C536009","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":869,"name":"Triple A syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}