{"orpha":3450,"name":"Weissenbacher-Zweymuller syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Pierre Robin sequence-fetal chondrodysplasia syndrome","Pierre Robin syndrome-fetal chondrodysplasia syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant otospondylomegaepiphyseal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-3450/","orphanet_url":"https://www.orpha.net/en/disease/detail/3450","names":{"fr":{"name":"Syndrome de Weissenbacher-Zweymuller","synonyms":["Syndrome de Pierre Robin-chondrodysplasie","Syndrome de séquence de Pierre Robin-chondrodysplasie"]},"de":{"name":"Weissenbacher-Zweymüller-Syndrom","synonyms":["Pierre Robin-Sequenz-fetale Chondrodysplasie-Syndrom","Pierre Robin-Syndrom-fetale Chondrodysplasie-Syndrom"]},"es":{"name":"Síndrome de Weissenbacher-Zweymuller","synonyms":["Síndrome de Pierre Robin-condrodisplasia fetal","Síndrome de secuencia de Pierre Robin-condrodisplasia fetal"]},"it":{"name":"Sindrome di Weissenbacher-Zweymuller","synonyms":["Displasia oto-spondilo-megaepifisaria eterozigote","OSMED, forma eterozigote","Sequenza di Pierre Robin - condrodisplasia fetale","Sindrome di Pierre Robin - condrodisplasia fetale"]},"nl":{"name":"Syndroom van Weissenbacher-Zweymuller","synonyms":["Pierre Robin sequentie - foetale chondrodysplasie-syndroom","Syndroom van Pierre Robin - foetale chondrodysplasie-syndroom"]},"pt":{"name":"Síndrome Weissenbacher-Zweymuller","synonyms":["Síndrome Pierre-Robin-condrodisplasia fetal","Síndrome de sequência Pierre-Robin-condrodisplasia fetal"]},"pl":{"name":"Zespół Weissenbachera i Zweymullera","synonyms":["Heterozygotyczna dysplazja uszno-kręgowo-nasadowa","Heterozygotyczna OSMED","Sekwencja Pierre'a i Robina - chondrodysplazja płodu","Zespół Pierre'a i Robina - chondrodysplazja płodu"]},"cs":{"name":"Weissenbacherův-Zweymullerův syndrom","synonyms":["Heterozygotní OSMED","Heterozygotní otospondylomegaepifyzeální dysplázie","Syndrom zahrnující Pierre Robinovu sekvenci a fetální chondrodysplázii","Syndrom zahrnující Pierre Robinův syndrom a fetální chondrodysplázii","Weissenbacher-Zweymullerův syndrom"]},"uk":{"name":"Синдром Вайсенбахера-Цвеймуллера","synonyms":["Синдром послідовності Пєра Робена - хондродисплазії плода","Синдром Пєра Робена - синдром хондродисплазії плода"]},"zh":{"name":"Weissenbacher-Zweymuller 综合征","synonyms":["Pierre Robin序列征-胎儿软骨发育不全综合征"]},"tr":{"name":"Weissenbacher-Zweymuller sendromu","synonyms":["Pierre Robin dizisi-fetal kondrodisplazi sendromu","Pierre Robin sendromu-fetal kondrodisplazi sendromu"]}},"xrefs":[{"source":"UMLS","code":"C1848488","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"4351","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":166100,"name":"Autosomal dominant otospondylomegaepiphyseal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}