{"orpha":1088,"name":"OBSOLETE: Short stature-heart defect-craniofacial anomalies syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Rommen-Mueller-Sybert syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-1088/","orphanet_url":"https://www.orpha.net/en/disease/detail/1088","names":{"fr":{"name":"OBSOLETE : Syndrome d'anomalies craniofaciales multiples-cardiopathie-retard de croissance","synonyms":["OBSOLETE : Syndrome de Rommen-Mueller-Sybert"]},"de":{"name":"OBSOLET: Kleinwuchs-Herzfehler-kraniofaziale Anomalien-Syndrom","synonyms":["OBSOLET: Rommen-Mueller-Sybert-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de talla baja-cardiopatía-anomalías craneofaciales","synonyms":["OBSOLETO: Síndrome de Rommen-Mueller-Sybert"]},"it":{"name":"OBSOLETO: Sindrome bassa statura-cardiopatia-anomalie craniofacciali","synonyms":["OBSOLETO: Sindrome di Rommen-Mueller-Sybert"]},"nl":{"name":"OBSOLEET: Kleine gestalte - hartdefect - craniofaciale anomalieën-syndroom","synonyms":["OBSOLEET: Syndroom van Rommen-Mueller-Sybert"]},"pt":{"name":"OBSOLETO: Síndrome de baixa estatura-defeito cardíaco-anomalias crânio-faciais"},"pl":{"name":"NIEAKTUALNE: Zespól niskiego wzrostu, wady serca i anomalii czaszkowo-twarzowej","synonyms":["NIEAKTUALNE: Zespół Rommena, Muellera i Syberta"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující malý vzrůst, srdeční defekt a kraniofaciální anomálie","synonyms":["NEAKTUÁLNÍ: Rommenův-Muellerův-Sybertův syndrom","NEAKTUÁLNÍ: Rommen-Mueller-Sybertův syndrom"]},"uk":{"name":"Синдром низького зросту - серцевої вади - черепно-лицьових аномалій","synonyms":["ЗАСТАРІЛО: Синдром Роммена-Мюллера-Сіберта"]},"zh":{"name":"废弃：身材矮小-心脏缺陷-颅面畸形综合征","synonyms":["Rommen-Mueller-Sybert综合征"]},"tr":{"name":"Eski adı: Kısa boy-kalp defekti-kraniyofasiyal anomaliler sendromu","synonyms":["Rommen-Mueller-Sybert sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102283,"name":"Multiple congenital anomalies/dysmorphic syndrome-intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}