<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/RktzgskoBxeRQy8BRut6Du">
  <rdfs:subClassOf rdf:resource="https://folio.openlegalstandard.org/RkvRD1NfpM4aO12DEEarGf"/>
  <rdfs:subClassOf rdf:resource="https://folio.openlegalstandard.org/RnmmbswQcOryRPEoDnHIbC"/>
  <rdfs:label>Huntington's Disease</rdfs:label>
  <skos:altLabel>Huntington's Chorea</skos:altLabel>
  <skos:definition>Huntington's disease is a progressive neurodegenerative disorder characterized by the gradual onset of motor dysfunction, cognitive decline, and psychiatric symptoms due to the degeneration of neurons in the basal ganglia. It is caused by a genetic mutation in the HTT gene, leading to a typical onset in middle adulthood and requiring ongoing medical and supportive care.</skos:definition>
</owl:Class>
