{"orpha":294925,"name":"Non-syndromic amelia","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-294925/","orphanet_url":"https://www.orpha.net/en/disease/detail/294925","names":{"fr":{"name":"Amélie non syndromique"},"de":{"name":"Amelie, nicht-syndromale"},"es":{"name":"Amelia no sindrómica"},"it":{"name":"Amelia non sindromica"},"nl":{"name":"Niet-syndromale amelie"},"pt":{"name":"Amelia não-sindrómica"},"pl":{"name":"Amelia niesyndromiczna"},"cs":{"name":"Amelie"},"uk":{"name":"Несиндромальна амелія"},"zh":{"name":"缺肢"},"tr":{"name":"Ameli"}},"xrefs":[{"source":"ICD-10","code":"Q73.0","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"17419","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5925013","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10001926","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":498461,"name":"Non-syndromic terminal transverse limb defect","classifications":[147,156,199]}],"children":[{"orpha":294969,"name":"Isolated amelia of lower limb","type":"Morphological anomaly"},{"orpha":294967,"name":"Isolated amelia of upper limb","type":"Morphological anomaly"},{"orpha":294971,"name":"Isolated tetra-amelia","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}