{"orpha":93974,"name":"Smith-Fineman-Myers 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 Alpha-thalassemia-X-linked intellectual disability syndrome","url":"https://raremap.alftech.space/d/ORPHA-93974/","orphanet_url":"https://www.orpha.net/en/disease/detail/93974","names":{"fr":{"name":"Syndrome de Smith-Fineman-Myers"},"de":{"name":"Smith-Fineman-Myers-Syndrom"},"es":{"name":"Síndrome de Smith-Fineman-Myers"},"it":{"name":"Sindrome di Smith-Fineman-Myers"},"nl":{"name":"Syndroom van Smith-Fineman-Myers"},"pt":{"name":"Síndrome de Smith-Fineman-Myers"},"pl":{"name":"Zespół Smitha, Finemana i Myersa"},"cs":{"name":"Smithův-Finemanův-Myersův syndrom","synonyms":["Smith-Fineman-Myersův syndrom"]},"uk":{"name":"Синдром Сміта-Файнмана-Майєрса"},"zh":{"name":"Smith-Fineman-Myers综合征"},"tr":{"name":"Smith-Fineman-Myers sendromu"}},"xrefs":[{"source":"UMLS","code":"C0796159","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"3521","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":847,"name":"X-linked alpha-thalassemia-intellectual disability syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}