{"iri":"https://folio.openlegalstandard.org/RktzgskoBxeRQy8BRut6Du","label":"Huntington's Disease","sub_class_of":["https://folio.openlegalstandard.org/RkvRD1NfpM4aO12DEEarGf","https://folio.openlegalstandard.org/RnmmbswQcOryRPEoDnHIbC"],"parent_class_of":[],"is_defined_by":null,"see_also":[],"comment":null,"deprecated":false,"preferred_label":null,"alternative_labels":["Huntington's Chorea"],"translations":{},"hidden_label":null,"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.","examples":[],"notes":[],"history_note":null,"editorial_note":null,"in_scheme":null,"identifier":null,"description":null,"source":null,"country":null}