{"orpha":206701,"name":"Bulbospinal muscular atrophy","type":"Category","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-206701/","orphanet_url":"https://www.orpha.net/en/disease/detail/206701","names":{"fr":{"name":"Amyotrophie bulbospinale"},"de":{"name":"Muskelatrophie, bulbospinale"},"es":{"name":"Atrofia muscular bulboespinal"},"it":{"name":"Atrofia muscolare bulbospinale"},"nl":{"name":"Bulbospinale spieratrofie","synonyms":["Bulbospinale musculaire atrofie"]},"pt":{"name":"Atrofia muscular bulbo-espinhal"},"pl":{"name":"Opuszkowo-rdzeniowy zanik mięśni"},"cs":{"name":"Bulbospinální svalová atrofie"},"uk":{"name":"Бульбоспинальна мязова атрофія"},"zh":{"name":"延髓肌萎缩"},"tr":{"name":"Bulbospinal kas atrofisi"}},"xrefs":[{"source":"MONDO","code":"0016113","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16113","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0393547","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98505,"name":"Genetic motor neuron disease","classifications":[156,181]}],"children":[{"orpha":206707,"name":"Bulbospinal muscular atrophy of adult","type":"Clinical group"},{"orpha":206704,"name":"Bulbospinal muscular atrophy of childhood","type":"Clinical group"},{"orpha":206710,"name":"Generalized bulbospinal muscular atrophy","type":"Clinical group"},{"orpha":207012,"name":"Spinal muscular atrophy associated with central nervous system anomaly","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}