{"orpha":171215,"name":"OBSOLETE: Low isolated anorectal malformation","type":"Morphological anomaly","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 Non-syndromic anorectal malformation","url":"https://raremap.alftech.space/d/ORPHA-171215/","orphanet_url":"https://www.orpha.net/en/disease/detail/171215","names":{"fr":{"name":"OBSOLETE : Malformation anorectale isolée basse"},"de":{"name":"OBSOLET: Anorektale Fehlbildung, tiefe Form"},"es":{"name":"OBSOLETO: Malformación anorrectal baja aislada"},"it":{"name":"OBSOLETO: Malformazione anorettale bassa isolata"},"nl":{"name":"OBSOLEET: Lage geïsoleerde anorectale malformatie"},"pt":{"name":"OBSOLETO: Malformação anoretal baixa isolada"},"pl":{"name":"NIEAKTUALNE: Wady odbytu i odbytnicy typu niskiego"},"cs":{"name":"NEAKTUÁLNÍ: Nízká anorektální malformace"},"uk":{"name":"ЗАСТАРІЛО: Низька ізольована аноректальна вада розвитку"},"zh":{"name":"孤立性低位肛门直肠畸形","definition":"孤立性低位肛门直肠畸形是一种罕见的遗传性非综合征型直肠肛门畸形，由于胚胎发育障碍所致，其主要临床表现为坐骨结节以下的肛门直肠畸形（e.g.,女性肛门前庭瘘、会阴瘘、肛门皮肤瘘和肛门狭窄），可出现胎粪排出障碍、发育不良和慢性便秘。"},"tr":{"name":"Düşük izole anorektal malformasyon"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":557,"name":"Non-syndromic anorectal malformation"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}