{"orpha":93546,"name":"Non-syndromic renal or urinary tract malformation","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-93546/","orphanet_url":"https://www.orpha.net/en/disease/detail/93546","names":{"fr":{"name":"Anomalie non syndromique du développement du rein et des voies urinaires"},"de":{"name":"Nieren/Harnwegsfehlbildung, nicht-syndromale"},"es":{"name":"Malformación no sindrómica del tracto urinario o renal"},"it":{"name":"Malformazione non sindromica del tratto urinario o renale"},"nl":{"name":"Niet-syndromale malformatie van nier of urinewegen"},"pt":{"name":"Malformação renal ou do trato urinário não sindromática"},"pl":{"name":"Niesyndromiczne malformacje nerek lub układu moczowego"},"cs":{"name":"Nesyndromická malformace ledvinného nebo močového traktu"},"uk":{"name":"Несиндромальні вади розвитку нирок або сечовивідних шляхів"},"zh":{"name":"非综合征型肾或尿路畸形"},"tr":{"name":"Sendromik olmayan böbrek veya idrar yolu malformasyonu"}},"xrefs":[{"source":"UMLS","code":"C5681585","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":1849,"name":"OBSOLETE: Infundibulopelvic stenosis-multicystic kidney syndrome","status":"inactive"},{"type":"Referred to","orpha":2190,"name":"OBSOLETE: Congenital hydronephrosis","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":506213,"name":"Rare disorder potentially indicated for kidney transplant","classifications":[233]},{"orpha":93545,"name":"Renal or urinary tract malformation","classifications":[147,188]}],"children":[{"orpha":93109,"name":"Congenital megacalycosis","type":"Morphological anomaly"},{"orpha":617,"name":"Congenital primary megaureter","type":"Morphological anomaly"},{"orpha":435743,"name":"Congenital urachal anomaly","type":"Category"},{"orpha":237,"name":"Duplication of urethra","type":"Morphological anomaly"},{"orpha":322,"name":"Exstrophy-epispadias complex","type":"Malformation syndrome"},{"orpha":289365,"name":"Familial vesicoureteral reflux","type":"Malformation syndrome"},{"orpha":435365,"name":"Fetal lower urinary tract obstruction","type":"Clinical group"},{"orpha":1309,"name":"Medullary sponge kidney","type":"Morphological anomaly"},{"orpha":238637,"name":"Megacystis-megaureter syndrome","type":"Disease"},{"orpha":1851,"name":"Multicystic dysplastic kidney","type":"Morphological anomaly"},{"orpha":2260,"name":"Oligomeganephronia","type":"Morphological anomaly"},{"orpha":411709,"name":"Renal agenesis","type":"Morphological anomaly"},{"orpha":93108,"name":"Renal dysplasia","type":"Morphological anomaly"},{"orpha":93101,"name":"Renal hypoplasia","type":"Morphological anomaly"},{"orpha":3033,"name":"Renal tubular dysgenesis","type":"Malformation syndrome"},{"orpha":652528,"name":"Supernumerary kidney","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}