{"orpha":98655,"name":"Lens shape anomaly","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-98655/","orphanet_url":"https://www.orpha.net/en/disease/detail/98655","names":{"fr":{"name":"Anomalie de forme du cristallin"},"de":{"name":"Linsenanomalie (Form)"},"es":{"name":"Anomalía en la forma de las lentes"},"it":{"name":"Anomalia della forma del cristallino"},"nl":{"name":"Lensvormanomalie"},"pt":{"name":"Anomalia da forma do cristalino"},"pl":{"name":"Nieprawidłowy kształt soczewki"},"cs":{"name":"Anomálie tvaru čočky"},"uk":{"name":"Аномалія форми кришталика"},"zh":{"name":"晶状体形状异常"},"tr":{"name":"Lens şekli anomalisi"}},"xrefs":[{"source":"UMLS","code":"C0158553","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98553,"name":"Developmental defect of the eye","classifications":[147]},{"orpha":183557,"name":"Genetic developmental defect of the eye","classifications":[156]},{"orpha":183607,"name":"Genetic lens and zonula anomaly","classifications":[156]},{"orpha":98639,"name":"Rare lens disease","classifications":[189]}],"children":[{"orpha":63,"name":"Alport syndrome","type":"Disease"},{"orpha":138,"name":"CHARGE syndrome","type":"Malformation syndrome"},{"orpha":2092,"name":"Focal dermal hypoplasia","type":"Malformation syndrome"},{"orpha":564,"name":"Meckel syndrome","type":"Malformation syndrome"},{"orpha":568,"name":"Microphthalmia, Lenz type","type":"Malformation syndrome"},{"orpha":783,"name":"Rubinstein-Taybi syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}