{"orpha":2569,"name":"Moore-Federman syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Dwarfism-stiff joint-ocular abnormalities syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Acromicric dysplasia","url":"https://raremap.alftech.space/d/ORPHA-2569/","orphanet_url":"https://www.orpha.net/en/disease/detail/2569","names":{"fr":{"name":"Syndrome de Moore-Federman","synonyms":["Syndrome de nanisme-raideur articulaire-anomalies oculaires"]},"de":{"name":"Moore-Federman-Syndrom","synonyms":["Kleinwuchs - eingeschränkte Gelenkmobilität - Augenanomalien"]},"es":{"name":"Síndrome de Moore-Federman","synonyms":["Síndrome de enanismo-contracturas articulares-anomalías oculares"]},"it":{"name":"Sindrome di Moore-Federman","synonyms":["Nanismo - rigidità articolare - anomalie oculari"]},"nl":{"name":"Syndroom van Moore-Federman","synonyms":["Dwerggroei - stijfheid van gewricht - oculaire afwijkingen-syndroom"]},"pt":{"name":"Síndrome Moore-Federman","synonyms":["Síndrome de nanismo-rigidez articular-anomalias oculares"]},"pl":{"name":"Zespół Moore'a i Federmana","synonyms":["Karłowatość - sztywność stawów - nieprawidłowości oczu"]},"cs":{"name":"Mooreův-Federmanův syndrom","synonyms":["Syndrom zahrnující trpaslictví, ztuhlé klouby a okulární abnormality","Moore-Federmanův syndrom"]},"uk":{"name":"Синдром Мура-Федермана","synonyms":["Синдром карликовості-ригідних суглобово-очних аномалій"]},"zh":{"name":"Moore-Federman综合征","synonyms":["Moore-Federman综合征"]},"tr":{"name":"Moore-Federman sendromu","synonyms":["Cücelik-sert eklem-oküler anormallikler sendromu"]}},"xrefs":[{"source":"OMIM","code":"127200","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0265349","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":969,"name":"Acromicric dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}