{"orpha":93458,"name":"Non-syndromic polydactyly, syndactyly and/or hyperphalangy","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-93458/","orphanet_url":"https://www.orpha.net/en/disease/detail/93458","names":{"fr":{"name":"Polydactylie, syndactylie et/ou hyperphalangie non syndromique"},"de":{"name":"Polydaktylie, Syndaktylie und/oder Hyperphalangie, nicht-syndromal"},"es":{"name":"Polidactilia, sindactilia y/o hiperfalangismo no sindrómico"},"it":{"name":"Polidattilia, sindattilia e/o iperfalangia non sindromica"},"nl":{"name":"Niet-syndromale polydactylie, syndactylie en/of hyperfalangie"},"pt":{"name":"Polidactialia, sindactilia e/ou hiperfalangismo não sindromáticos"},"pl":{"name":"Polidaktylia, syndaktylia i/lub hiperfalangia"},"cs":{"name":"Nesyndromické polydaktylie, syndaktylie a/nebo hyperfalangie"},"uk":{"name":"Несиндромна полідактилія, синдактилія та/або гіперфалангія"},"zh":{"name":"非综合征型多指（趾）和/或并指（趾）"},"tr":{"name":"Non-Sendromik polidaktili, sindaktili ve / veya hiperfalji"}},"xrefs":[{"source":"UMLS","code":"C5681597","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":404571,"name":"Dysostosis of genetic origin with limb anomaly as a major feature","classifications":[156]},{"orpha":364568,"name":"Dysostosis with limb anomaly as a major feature","classifications":[147,199]},{"orpha":109011,"name":"Non-syndromic limb malformation","classifications":[147,156]}],"children":[{"orpha":295002,"name":"Isolated hyperphalangy","type":"Morphological anomaly"},{"orpha":2913,"name":"Non-syndromic polydactyly","type":"Category"},{"orpha":90025,"name":"Non-syndromic syndactyly","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}