{"orpha":171208,"name":"OBSOLETE: Intermediate 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-171208/","orphanet_url":"https://www.orpha.net/en/disease/detail/171208","names":{"fr":{"name":"OBSOLETE : Malformation anorectale isolée intermédiaire"},"de":{"name":"OBSOLET: Anorektale Fehlbildung, intermediäre Form"},"es":{"name":"OBSOLETO: Malformación anorrectal intermedia aislada"},"it":{"name":"OBSOLETO: Malformazione anorettale intermedia isolata"},"nl":{"name":"OBSOLEET: Intermediaire geïsoleerde anorectale malformatie"},"pt":{"name":"OBSOLETO: Malformação anoretal intermédia isolada"},"pl":{"name":"NIEAKTUALNE: Wady odbytu i odbytnicy typu pośredniego"},"cs":{"name":"NEAKTUÁLNÍ: Střední anorektální malformace"},"uk":{"name":"ЗАСТАРІЛО: Помірно виражена ізольована аноректальна вада розвитку"},"zh":{"name":"孤立性中位肛门直肠畸形","definition":"孤立性中间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，其主要临床表现为耻骨线和坐骨结节之间的肛门直肠畸形（e.g.,女性直肠前庭瘘和直肠阴道瘘，男性直肠瘘、肛门发育不全），可表现为胎粪排出障碍、发育不良和反复尿路感染。"},"tr":{"name":"Orta derecede 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}