{"orpha":2292,"name":"OBSOLETE: Congenital bowing of long bones-short stature-dolichomacrocephaly-ocular hypertelorism syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Campomelic dysplasia and related disorders","url":"https://raremap.alftech.space/d/ORPHA-2292/","orphanet_url":"https://www.orpha.net/en/disease/detail/2292","names":{"fr":{"name":"OBSOLETE : Syndrome d'incurvation congénitale des os longs-petite taille-dolichomacrocéphalie-hypertélorisme oculaire","synonyms":["OBSOLETE : Incurvation des os longs"]},"de":{"name":"OBSOLET: Kongenitale Verkrümmung der Röhrenknochen-Kleinwuchs-Dolichomakrozephalie-okulärer Hypertelorismus-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de incurvación congénita de huesos largos-talla baja-dolicomacrocefalia-hipertelorismo ocular"},"it":{"name":"OBSOLETO: Sindrome da incurvamento congenito delle ossa lunghe-bassa statura-dolicomacrocefalia-ipertelorismo oculare"},"nl":{"name":"OBSOLEET: Congenitale kromstand van pijpbeenderen - kleine gestalte - dolichomacrocefalie - oculair hypertelorisme-syndroom"},"pt":{"name":"OBSOLETO: Síndrome de encurvamento congénito dos ossos longos-baixa estatura-dolicomacrocefalia-hipertelorismo ocular"},"pl":{"name":"NIEAKTUALNE: Wrodzona łukowatość kości długich","synonyms":["NIEAKTUALNE: Wrodzony zespół wygięcia kości długich, niskiego wzrostu, dolichomakrocefalii i hiperteloryzmu ocznego"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující vrozené ohnutí dlouhých kostí, malý vzrůst, dolichomakrocefalii a hypertelorismus očí"},"uk":{"name":"ЗАСТАРІЛО: Синдром вродженої деформації довгих кісток - низького зросту - доліхомакроцефалії - очного гіпертелоризму"},"zh":{"name":"先天性长骨弯曲"},"tr":{"name":"Uzun kemiklerin doğumsal eğilmesi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93439,"name":"Campomelic dysplasia and related disorders"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}