{"orpha":1773,"name":"Sacrococcygeal dysgenesis association","type":"Malformation syndrome","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 Caudal regression syndrome","url":"https://raremap.alftech.space/d/ORPHA-1773/","orphanet_url":"https://www.orpha.net/en/disease/detail/1773","names":{"fr":{"name":"Dysgénésie sacro-coccygienne"},"de":{"name":"Dysgenesie, sakrokokzygeale"},"es":{"name":"Disgenesia sacrococcígea"},"it":{"name":"Disgenesia sacro-coccigea"},"nl":{"name":"Sacrococcygeale dysgenesie-associatie"},"pt":{"name":"Disgenesia sacrococcígea"},"pl":{"name":"Asocjacja dysgenezji krzyżowo-guzicznej"},"cs":{"name":"Sakrokokcygeální dysgeneze"},"uk":{"name":"Асоціація крижово-куприкової дисгенезії"},"zh":{"name":"骶尾骨联合发育不全"},"tr":{"name":"Sakrokoksigeal disgenezi ilişkisi"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":3027,"name":"Caudal regression syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}