{"orpha":498467,"name":"Non-syndromic postaxial polydactyly","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-498467/","orphanet_url":"https://www.orpha.net/en/disease/detail/498467","names":{"fr":{"name":"Polydactylie post-axiale non syndromique"},"de":{"name":"Polydaktylie, postaxiale, nicht-syndromale"},"es":{"name":"Polidactilia postaxial no sindrómica"},"it":{"name":"Polidattilia postassiale non sindromica"},"nl":{"name":"Niet-syndromale postaxiale polydactylie"},"pt":{"name":"Polidactilia pós-axial não sindromática"},"pl":{"name":"Niesyndromiczna polidaktylia zaosiowa"},"cs":{"name":"Nesyndromická postaxiální polydaktylie"},"uk":{"name":"Несиндромальна постаксіальна полідактилія"},"zh":{"name":"非综合征性轴后多指症"},"tr":{"name":"Sendromik olmayan postaksiyal polidaktili"}},"xrefs":[{"source":"UMLS","code":"C5681228","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":294942,"name":"OBSOLETE: Postaxial polydactyly of fingers","status":"inactive"},{"type":"Referred to","orpha":295008,"name":"OBSOLETE: Postaxial polydactyly of toes","status":"inactive"},{"type":"Referred to","orpha":295179,"name":"OBSOLETE: Postaxial polydactyly of toes, unilateral","status":"inactive"},{"type":"Referred to","orpha":295181,"name":"OBSOLETE: Postaxial polydactyly of toes, bilateral","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":2913,"name":"Non-syndromic polydactyly","classifications":[147,156,199]}],"children":[{"orpha":93334,"name":"Postaxial polydactyly type A","type":"Morphological anomaly"},{"orpha":93335,"name":"Postaxial polydactyly type B","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}