{"orpha":498477,"name":"Ectrodactyly with and without other manifestations","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-498477/","orphanet_url":"https://www.orpha.net/en/disease/detail/498477","names":{"fr":{"name":"Ectrodactylie avec et sans autres manifestations"},"de":{"name":"Ektrodaktylie mit und ohne weitere Manifestationen"},"es":{"name":"Ectrodactilia con y sin otras manifestaciones"},"it":{"name":"Ectrodattilia con/senza altri segni clinici"},"nl":{"name":"Ectrodactylie met en zonder andere manifestaties"},"pt":{"name":"Ectrodactilia com e sem outras manifestações"},"pl":{"name":"Ektrodaktylia z i bez innych objawów"},"cs":{"name":"Ektrodaktylie s/bez dalších manifestací"},"uk":{"name":"Ектродактилія з іншими проявами та без них"},"zh":{"name":"先天性缺指合并或不合并其他畸形"},"tr":{"name":"Diğer belirtilerle seyreden ve belirtiler göstermeyen ektrodaktili"}},"xrefs":[{"source":"UMLS","code":"C5681242","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]}],"children":[{"orpha":978,"name":"ADULT syndrome","type":"Malformation syndrome"},{"orpha":1406,"name":"Charlie M syndrome","type":"Malformation syndrome"},{"orpha":1896,"name":"EEC syndrome","type":"Malformation syndrome"},{"orpha":1897,"name":"EEM syndrome","type":"Malformation syndrome"},{"orpha":708043,"name":"Ectodermal dysplasia with oligodontia-hand and foot malformation-hypoplastic nipples","type":"Malformation syndrome"},{"orpha":1892,"name":"Ectrodactyly-polydactyly syndrome","type":"Malformation syndrome"},{"orpha":1118,"name":"Fibular aplasia-ectrodactyly syndrome","type":"Malformation syndrome"},{"orpha":1986,"name":"Gollop-Wolfgang complex","type":"Malformation syndrome"},{"orpha":2117,"name":"Hartsfield syndrome","type":"Malformation syndrome"},{"orpha":2440,"name":"Isolated split hand-split foot malformation","type":"Malformation syndrome"},{"orpha":69085,"name":"Limb-mammary syndrome","type":"Malformation syndrome"},{"orpha":2439,"name":"Patterson-Stevenson-Fontaine syndrome","type":"Malformation syndrome"},{"orpha":3329,"name":"Tibial aplasia-ectrodactyly syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}