{"orpha":1301,"name":"Bronchiectasis-oligospermia syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Young syndrome","url":"https://raremap.alftech.space/d/ORPHA-1301/","orphanet_url":"https://www.orpha.net/en/disease/detail/1301","names":{"fr":{"name":"Syndrome de bronchiectasie-oligospermie"},"de":{"name":"Bronchiektasie mit Oligospermie"},"es":{"name":"Síndrome de bronquiectasias-oligospermia"},"it":{"name":"Bronchiectasia oligospermia"},"nl":{"name":"Bronchiëctasie - oligospermie-syndroom"},"pt":{"name":"Síndrome de bronquiectasia-oligospermia"},"pl":{"name":"Rozstrzenie oskrzeli - oligospermia"},"cs":{"name":"Syndrom zahrnující bronchiektázie a oligospermii"},"uk":{"name":"Синдром бронхоектазів-олігоспермії"},"zh":{"name":"支气管扩张-少弱精子症综合征"},"tr":{"name":"Bronşiektazi-oligospermi sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":3471,"name":"Young syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}