{"@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/homoit0002861","dc:identifier":"homoit0002861","skos:prefLabel":[{"@language":"en","@value":"Jacobs syndrome"},{"@language":"es","@value":"Síndrome de Jakob"}],"skos:altLabel":[{"@language":"en","@value":"47XYY"},{"@language":"en","@value":"XYY syndrome"},{"@language":"es","@value":"Síndrome XYY"},{"@language":"es","@value":"Síndrome del supermacho"}],"rdfs:comment":[{"@language":"en","@value":"People with Jacobs syndrome develop with an extra Y chromosome. They might not have any obvious physical variations as a result, or they may be taller than usual or have other identifiable differences that do not relate to sex characteristics. Some people with Jacobs syndrome may also have a smaller-than-typical penis or scrotum, hypospadias, and/or undescended testicles."},{"@language":"es","@value":"Las personas con síndrome de Jakob se desarrollan con un cromosoma Y adicional. Como resultado, es posible que no tengan variaciones físicas obvias, o puede que sean más altas de lo habitual o tener otras diferencias identificables que no se relacionan con las características sexuales. Algunas personas con síndrome de Jakob también pueden tener un pene o escroto más pequeño de lo normal, hipospadias y/o testículos no descendidos."}],"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":[]}