{"orpha":180154,"name":"Septate vagina","type":"Morphological anomaly","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":"A rare vaginal malformation characterized by the presence of a complete or incomplete longitudinal or transverse septum in the vagina due to disrupted fusion or canalization of the solid vaginal plate during embryogenesis. Signs and symptoms depend on the type of septum.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-180154/","orphanet_url":"https://www.orpha.net/en/disease/detail/180154","names":{"fr":{"name":"Vagin cloisonné","definition":"Malformation vaginale rare caractérisée par la présence d'une cloison longitudinale ou transversale complète ou incomplète dans le vagin, due à anomalie de la fusion de la zone d'accolement des canaux pendant l'embryogenèse. Les signes cliniques et les symptômes dépendent du type de l'anomalie du septum."},"de":{"name":"Vagina, septierte","synonyms":["Vaginalseptum"],"definition":"Eine seltene Fehlbildung der Vagina, die durch das Vorhandensein eines vollständigen oder unvollständigen Längs- oder Querseptums in der Vagina gekennzeichnet ist, das auf eine gestörte Verschmelzung oder Kanalisierung der festen Vaginalplatte während der Embryogenese zurückzuführen ist. Die Anzeichen und Symptome hängen von der jeweiligen Ausprägung des Septums ab."},"es":{"name":"Vagina septada","definition":"Es una malformación poco frecuente de la vagina caracterizada por la presencia de un septo vaginal longitudinal o transversal completo o incompleto debido a una alteración de la fusión o canalización de la placa vaginal sólida durante la embriogénesis. Los signos y síntomas dependen del tipo de septo."},"it":{"name":"Vagina settata","definition":"Si tratta di una malformazione vaginale rara, caratterizzata dalla presenza nella vagina di un setto longitudinale o trasversale, completo o incompleto, secondario alla mancata fusione o canalizzazione del piatto vaginale solido durante l'embriogenesi. I sintomi dipendono dalla tipologia del setto."},"nl":{"name":"Septum van vagina","synonyms":["Vaginaal septum"],"definition":"Een zeldzame malformatie van vagina, gekarakteriseerd door aanwezigheid van een volledig of onvolledig longitudinaal of transversaal septum in vagina als gevolg van verstoorde fusie of kanalisatie van de vaginale plaat tijdens embryogenese. Verschijnselen en symptomen zijn afhankelijk van het type van septum."},"pt":{"name":"Vagina septada"},"pl":{"name":"Przegroda pochwy"},"cs":{"name":"Septovaná vagina"},"uk":{"name":"Перегороджена піхва","definition":"A rare vaginal malformation characterized by the presence of a complete or incomplete longitudinal or transverse septum in the vagina due to disrupted fusion or canalization of the solid vaginal plate during embryogenesis. Signs and symptoms depend on the type of septum."},"zh":{"name":"有隔阴道"},"tr":{"name":"Septate vajina"}},"xrefs":[{"source":"ICD-10","code":"Q52.1","qualifier":"NTBT","icd_relation":"inclusion","validated":true},{"source":"ICD-11","code":"LB42.1","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1699475508"},{"source":"MONDO","code":"0015848","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0266411","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":180151,"name":"Rare vaginal malformation","classifications":[147,185,201,205,233]}],"children":[{"orpha":180157,"name":"Longitudinal vaginal septum","type":"Clinical subtype"},{"orpha":180160,"name":"Transverse vaginal septum","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}