{"orpha":522534,"name":"Lacrimal drainage system anomaly of genetic origin","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-522534/","orphanet_url":"https://www.orpha.net/en/disease/detail/522534","names":{"fr":{"name":"Anomalie de l'appareil excréteur du système lacrymal d'origine génétique"},"de":{"name":"Genetisch bedingte Anomalie der ableitenden Tränenwege"},"es":{"name":"Anomalía del sistema de drenaje lagrimal de origen genético"},"it":{"name":"Anomalia del sistema di drenaggio lacrimale di origine genetica"},"nl":{"name":"Anomalie van lacrimaal drainagesysteem van genetische oorsprong","synonyms":["Anomalie van traanafvoersysteem van genetische oorsprong"]},"pt":{"name":"Anomalia do sistema de drenagem lacrimal de origem genética"},"pl":{"name":"Wada układu odprowadzającego łzy uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněná anomálie exkrečního aparátu slzných cest"},"uk":{"name":"Генетично обумовлена аномалія сльозової системи"},"zh":{"name":"遗传性排泪系统异常"},"tr":{"name":"Genetik kaynaklı lakrimal drenaj sistemi anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5681422","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183557,"name":"Genetic developmental defect of the eye","classifications":[156]},{"orpha":522532,"name":"Rare genetic disorder of the lacrimal apparatus","classifications":[156]}],"children":[{"orpha":451612,"name":"Familial congenital nasolacrimal duct obstruction","type":"Morphological anomaly"},{"orpha":519274,"name":"Syndromic lacrimal system disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}