{"orpha":498491,"name":"Non-syndromic complete hemimelia","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-498491/","orphanet_url":"https://www.orpha.net/en/disease/detail/498491","names":{"fr":{"name":"Hémimélie complète non syndromique"},"de":{"name":"Hemimelie, komplette, nicht-syndromale"},"es":{"name":"Hemimelia completa no sindrómica"},"it":{"name":"Emimelia completa non sindromica"},"nl":{"name":"Niet-syndromale volledige hemimelie"},"pt":{"name":"Hemimelia completa não-sindrómica"},"pl":{"name":"Całkowity niedorozwój kończyny","synonyms":["Niesyndromiczna całkowita hemimelia"]},"cs":{"name":"Kompletní hemimelie"},"uk":{"name":"Несиндромальна повна гемімелія"},"zh":{"name":"完全性半肢畸形"},"tr":{"name":"Tam hemimeli"}},"xrefs":[{"source":"MONDO","code":"0850030","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5925041","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":294979,"name":"Isolated absence of both forearm and hand","type":"Morphological anomaly"},{"orpha":294981,"name":"Isolated absence of both lower leg and foot","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}