{"orpha":965,"name":"Acromegaloid facial appearance 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 Cantú syndrome","url":"https://raremap.alftech.space/d/ORPHA-965/","orphanet_url":"https://www.orpha.net/en/disease/detail/965","names":{"fr":{"name":"Syndrome du faciès acromégaloïde"},"de":{"name":"Syndrom der akromegalen Gesichtszüge","synonyms":["Akromegaloides Gesichtsbild-Syndrom"]},"es":{"name":"Síndrome de facies acromegaloide"},"it":{"name":"Facies acromegaloide"},"nl":{"name":"Acromegaloïd aangezichtssyndroom"},"pt":{"name":"Síndrome de facies acromegalóide"},"pl":{"name":"Zespół akromegaloidalnego wyglądu twarzy"},"cs":{"name":"Syndrom akromegaloidně vyhlížejícího obličeje"},"uk":{"name":"Синдром акромегалоїдного вигляду обличчя"},"zh":{"name":"肢端肥大样面容综合征"},"tr":{"name":"Akromegaloid yüz görünüm sendromu"}},"xrefs":[{"source":"OMIM","code":"102150","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C535655","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0796280","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"501","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":1517,"name":"Cantú syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}