{"orpha":498461,"name":"Non-syndromic terminal transverse limb defect","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-498461/","orphanet_url":"https://www.orpha.net/en/disease/detail/498461","names":{"fr":{"name":"Anomalie réductionnelle transverse non syndromique des membres"},"de":{"name":"Extremitätendefekt, terminaler transversaler, nicht-syndromaler"},"es":{"name":"Defecto transverso terminal de las extremidades no sindrómico"},"it":{"name":"Difetto trasversale non sindromico della porzione terminale degli arti"},"nl":{"name":"Niet-syndromaal terminaal transversaal ledemaatdefect"},"pt":{"name":"Defeito terminal transverso do membro não-sindrómico"},"pl":{"name":"Niesyndromiczna wada poprzeczna końcowego odcinka kończyny"},"cs":{"name":"Terminální příčný defekt končetiny"},"uk":{"name":"Несиндромальний кінцевий поперечний дефект кінцівки"},"zh":{"name":"末端横断性肢体缺陷"},"tr":{"name":"Terminal enine ekstremite defekti"}},"xrefs":[{"source":"UMLS","code":"C5925039","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":1034,"name":"OBSOLETE: Amniotic bands","status":"inactive"},{"type":"Referred to","orpha":93937,"name":"OBSOLETE: Terminal transverse defects of arm","status":"inactive"},{"type":"Referred to","orpha":294990,"name":"OBSOLETE: Congenital absence/hypoplasia of fingers excluding thumb","status":"inactive"},{"type":"Referred to","orpha":295114,"name":"OBSOLETE: Congenital absence/hypoplasia of fingers excluding thumb, bilateral","status":"inactive"},{"type":"Referred to","orpha":295116,"name":"OBSOLETE: Adactyly of foot, unilateral","status":"inactive"},{"type":"Referred to","orpha":295118,"name":"OBSOLETE: Adactyly of foot, bilateral","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93457,"name":"Non-syndromic limb reduction defect","classifications":[147,156,199]}],"children":[{"orpha":973,"name":"Isolated absence/hypoplasia of fingers excluding thumb, unilateral","type":"Morphological anomaly"},{"orpha":294983,"name":"Isolated acheiria","type":"Morphological anomaly"},{"orpha":931,"name":"Isolated acheiropodia","type":"Morphological anomaly"},{"orpha":294986,"name":"Isolated apodia","type":"Morphological anomaly"},{"orpha":294925,"name":"Non-syndromic amelia","type":"Clinical group"},{"orpha":498491,"name":"Non-syndromic complete hemimelia","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}