{"orpha":306773,"name":"Hyperekplexia","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-306773/","orphanet_url":"https://www.orpha.net/en/disease/detail/306773","names":{"fr":{"name":"Hyperexplexie"},"de":{"name":"Hyperekplexie"},"es":{"name":"Hiperekplexia","synonyms":["Hiperecplexia","Hiperplexia"]},"it":{"name":"Iperekplexia"},"nl":{"name":"Hyperekplexie"},"pt":{"name":"Hiperecplexia"},"pl":{"name":"Hiperekpleksja"},"cs":{"name":"Hyperekplexie","synonyms":["Choroby s úlekovými reakcemi"]},"uk":{"name":"Гіперекплексія"},"zh":{"name":"过度惊吓反应症"},"tr":{"name":"Hiperekpleksi"}},"xrefs":[{"source":"MONDO","code":"0017658","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17658","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D000071017","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10058271","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":102003,"name":"Rare movement disorder","classifications":[181]}],"children":[{"orpha":3197,"name":"Hereditary hyperekplexia","type":"Disease"},{"orpha":163985,"name":"Hyperekplexia-epilepsy syndrome","type":"Disease"},{"orpha":306776,"name":"Sporadic hyperekplexia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}