{"@context":{"skos":"http://www.w3.org/2004/02/skos/core#","dc":"http://purl.org/dc/terms/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","xsd":"http://www.w3.org/2001/XMLSchema#"},"@id":"https://homosaurus.org/v4/homoit0002865","dc:identifier":"homoit0002865","skos:prefLabel":[{"@language":"en","@value":"Mayer-Rokitansky-Küster-Hauser syndrome"},{"@language":"es","@value":"Síndrome de Mayer-Rokitansky-Küster-Hauser"},{"@language":"nl","@value":"Mayer-Rokitansky-Küster-Hauser syndroom"}],"skos:altLabel":[{"@language":"en","@value":"MRKH syndrome "},{"@language":"en","@value":"Müllerian agenesis"},{"@language":"en","@value":"Müllerian duct anomalies"},{"@language":"en","@value":"Müllerian duct variations"}],"rdfs:comment":[{"@language":"en","@value":"Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome occurs when a person's Müllerian ducts, which typically become the uterus and upper portion of the vagina during fetal development, do not develop in the typical way. People with MRKH have XX chromosomes and are usually born with a vulva and either a vagina that is shorter than typical or no vagina. They usually do not have a cervix and may have a partial uterus (uterine remnant) or no uterus. They often do not mensturate but may experience cyclic pain if they have a uterine remnant with endometrial lining, and they can develop menstruation-related conditions like endometriosis."},{"@language":"es","@value":"El síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH, por sus siglas en inglés) ocurre cuando los conductos müllerianos de una persona, que normalmente se convierten en el útero y la parte superior de la vagina durante el desarrollo fetal, no se desarrollan de la manera típica. Las personas con MRKH tienen cromosomas XX y generalmente nacen con una vulva y una vagina más corta de lo normal o sin vagina. Por lo general, no tienen cuello uterino y pueden tener un útero parcial (restos uterinos) o ningún útero. A menudo no menstrúan, pero pueden experimentar dolor cíclico si tienen un remanente uterino con tejido endometrial y pueden desarrollar condiciones relacionadas con la menstruación, como la endometriosis."},{"@language":"nl","@value":"Mayer-Rokitansky-Küster-Hauser (MRKH)-syndroom treedt op wanneer de Mülleriaanse kanalen van een persoon, die tijdens de ontwikkeling van de foetus doorgaans de baarmoeder en het bovenste gedeelte van de vagina worden, zich niet op de typische manier ontwikkelen. Personen met MRKH hebben XX chromosomen en worden meestal geboren met een vulva en een vagina die korter is dan normaal, of zonder vagina. Ze hebben meestal geen baarmoederhals en kunnen een gedeeltelijke baarmoeder (baarmoederrest) of geen baarmoeder hebben. Ze menstureren vaak niet, maar kunnen cyclische pijn ervaren als ze een baarmoederrest met endometriumslijmvlies hebben, en ze kunnen menstruatiegerelateerde aandoeningen ontwikkelen, zoals endometriose."}],"skos:broader":[{"@id":"https://homosaurus.org/v4/homoit0000669","skos:prefLabel":{"@language":"en","@value":"Intersex variations"}}],"skos:narrower":[{"@id":"https://homosaurus.org/v4/homoit0002880","skos:prefLabel":{"@language":"en","@value":"Type 1 Mayer-Rokitansky-Küster-Hauser syndrome"}},{"@id":"https://homosaurus.org/v4/homoit0002882","skos:prefLabel":{"@language":"en","@value":"Type 2 Mayer-Rokitansky-Küster-Hauser syndrome"}}],"skos:hasTopConcept":{"@id":"https://homosaurus.org/v4/homoit0001269"},"dc:issued":{"@type":"xsd:date","@value":"2023-06-28"},"dc:modified":{"@type":"xsd:date","@value":"2025-02-23"},"@type":"skos:Concept","skos:inScheme":{"@id":"https://homosaurus.org/v3"},"skos:changeNote":"Version 5.0.3","skos:related":[],"dc:replaces":[],"dc:isReplacedBy":[]}