{"orpha":163988,"name":"OBSOLETE: Developmental delay-deafness syndrome, Hildebrand type","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 Xq21 microdeletion syndrome","url":"https://raremap.alftech.space/d/ORPHA-163988/","orphanet_url":"https://www.orpha.net/en/disease/detail/163988","names":{"fr":{"name":"OBSOLETE : Syndrome de retard de développement-surdité, type Hildebrand"},"de":{"name":"OBSOLET: Entwicklungsverzögerung - Schwerhörigkeit, Typ Hildebrand"},"es":{"name":"OBSOLETO: Síndrome de retraso del desarrollo-sordera, tipo Hildebrand"},"it":{"name":"OBSOLETO: Ritardo dello sviluppo - sordità, tipo Hildebrand"},"nl":{"name":"OBSOLEET: Ontwikkelingsachterstand - doofheid-syndroom, Hildebrand-type"},"pt":{"name":"OBSOLETO: Síndrome de perturbação do desenvolvimento-surdez, tipo Hildebrand"},"pl":{"name":"NIEAKTUALNE: Opóznienienie rozwoju - gluchota, typ Hildebranda"},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující opožděný vývoj a hluchotu, Hildebrandův typ"},"uk":{"name":"ЗАСТАРІЛО: Синдром затримки розвитку-глухоти, тип Гільдебранда"},"zh":{"name":"弃用: Hildebrand 型发育迟缓性耳聋综合征"},"tr":{"name":"Eski adı: gelişme geriliği-sağırlık sendromu, Hildebrand tipi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":1435,"name":"Xq21 microdeletion syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}