{"orpha":206704,"name":"Bulbospinal muscular atrophy of childhood","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-206704/","orphanet_url":"https://www.orpha.net/en/disease/detail/206704","names":{"fr":{"name":"Amyotrophie bulbospinale de l'enfant"},"de":{"name":"Muskelatrophie, bulbospinale, des Kindes"},"es":{"name":"Atrofia muscular bulboespinal infantil"},"it":{"name":"Atrofia muscolare bulbospinale del bambino"},"nl":{"name":"Bulbospinale spieratrofie bij kinderen","synonyms":["Bulbospinale musculaire atrofie bij kinderen"]},"pt":{"name":"Atrofia muscular bulbo-espinhal da infância"},"pl":{"name":"Opuszkowo-rdzeniowy zanik mięśni dzieci"},"cs":{"name":"Bulbospinální svalová atrofie dětského věku"},"uk":{"name":"Дитяча бульбоспінальна мязова атрофія"},"zh":{"name":"儿童期延髓肌萎缩"},"tr":{"name":"Çocuklukta bulbospinal kas atrofisi"}},"xrefs":[{"source":"MONDO","code":"16114","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680797","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":97229,"name":"Riboflavin transporter deficiency","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}