{"orpha":206710,"name":"Generalized bulbospinal muscular atrophy","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-206710/","orphanet_url":"https://www.orpha.net/en/disease/detail/206710","names":{"fr":{"name":"Amyotrophie spinale généralisée"},"de":{"name":"Muskelatrophie, bulbospinale generalisierte"},"es":{"name":"Atrofia muscular bulboespinal generalizada"},"it":{"name":"Atrofia muscolare bulbospinale generalizzata"},"nl":{"name":"Gegeneraliseerde bulbospinale spieratrofie","synonyms":["Gegeneraliseerde bulbospinale musculaire atrofie"]},"pt":{"name":"Atrofia muscular bulbo-espinhal generalizada"},"pl":{"name":"Uogólniony opuszkowo-rdzeniowy zanik mięśni"},"cs":{"name":"Generalizovaná bulbospinální svalová atrofie"},"uk":{"name":"Генералізована бульбоспинальна мязова атрофія"},"zh":{"name":"全身性延髓肌萎缩"},"tr":{"name":"jeneralize bulbospinal kas atrofisi"}},"xrefs":[{"source":"MONDO","code":"16116","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680795","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":206701,"name":"Bulbospinal muscular atrophy","classifications":[156,181]}],"children":[{"orpha":206580,"name":"Autosomal recessive lower motor neuron disease with childhood onset","type":"Disease"},{"orpha":1217,"name":"Spinal atrophy-ophthalmoplegia-pyramidal syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}