{"@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/homoit0002883","dc:identifier":"homoit0002883","skos:prefLabel":[{"@language":"en","@value":"Vaginal atresia"},{"@language":"es","@value":"Atresia vaginal"}],"rdfs:comment":[{"@language":"en","@value":"People with this variation may be born without a vaginal opening, a shallow “dimple” where an opening would typically be, or a vaginal opening that is fused or blocked by fibrous tissue. People with vaginal atresia often have a typical upper vaginal canal (along with a typical uterus, cervix, fallopian tubes, and ovaries) with differences in the lower portion of the vagina only."},{"@language":"es","@value":"Las personas con esta variación pueden nacer sin una abertura vaginal, un \"hoyuelo\" poco profundo donde normalmente estaría una abertura, o una abertura vaginal fusionada o bloqueada por tejido fibroso. Las personas con atresia vaginal a menudo tienen un canal vaginal superior típico (junto con un útero, cuello uterino, trompas de Falopio y ovarios típicos) con diferencias solo en la porción inferior de la vagina."}],"skos:broader":[{"@id":"https://homosaurus.org/v4/homoit0000669","skos:prefLabel":{"@language":"en","@value":"Intersex variations"}}],"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 4.2.0","skos:narrower":[],"skos:related":[],"dc:replaces":[],"dc:isReplacedBy":[]}