{"orpha":457074,"name":"Congenital nemaline myopathy","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-457074/","orphanet_url":"https://www.orpha.net/en/disease/detail/457074","names":{"fr":{"name":"Myopathie à némaline congénitale"},"de":{"name":"Nemalin-Myopathie, kongenitale"},"es":{"name":"Miopatía nemalínica congénita"},"it":{"name":"Miopatia nemalinica congenita"},"nl":{"name":"Congenitale nemaline myopathie"},"pt":{"name":"Miopatia nemalina congénita"},"pl":{"name":"Wrodzona miopatia nemalinowa"},"cs":{"name":"Kongenitální nemalinová myopatie","synonyms":["Vrozená nemalinová myopatie"]},"uk":{"name":"Вроджена немалінова міопатія"},"zh":{"name":"先天性线形体肌病"},"tr":{"name":"Doğumsal nemalin miyopati"}},"xrefs":[{"source":"MONDO","code":"18701","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1268589","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":97245,"name":"Congenital myopathy","classifications":[156,181]}],"children":[{"orpha":98902,"name":"Amish nemaline myopathy","type":"Disease"},{"orpha":171433,"name":"Intermediate nemaline myopathy","type":"Disease"},{"orpha":171430,"name":"Severe congenital nemaline myopathy","type":"Disease"},{"orpha":171436,"name":"Typical nemaline myopathy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}