<owl:Class xmlns="https://folio.openlegalstandard.org/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:v1="http://www.loc.gov/mads/rdf/v1#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" xmlns:folio="https://folio.openlegalstandard.org/" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:skos="http://www.w3.org/2004/02/skos/core#" rdf:about="https://folio.openlegalstandard.org/RBm4FfOtNNc2YXqnz3Pkqce">
  <rdfs:subClassOf rdf:resource="https://folio.openlegalstandard.org/R8LxIR1bsgFd3td2G24G3mq"/>
  <rdfs:label>Fragile X Syndrome</rdfs:label>
  <skos:altLabel>FXS</skos:altLabel>
  <skos:altLabel>Fragile X Mental Retardation Syndrome</skos:altLabel>
  <skos:definition>Fragile X Syndrome is a genetic disorder caused by a mutation on the FMR1 gene located on the X chromosome. This mutation leads to a lack of the fragile X mental retardation protein (FMRP), which is crucial for normal brain development.</skos:definition>
</owl:Class>
