{"orpha":99914,"name":"Gynandroblastoma","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-99914/","orphanet_url":"https://www.orpha.net/en/disease/detail/99914","names":{"fr":{"name":"Gynandroblastome"},"de":{"name":"Gynandroblastom"},"es":{"name":"Ginandroblastoma"},"it":{"name":"Ginandroblastoma"},"nl":{"name":"Gynandroblastoom"},"pt":{"name":"Ginandroblastoma"},"pl":{"name":"Gynandroblastoma"},"cs":{"name":"Gynandroblastom"},"uk":{"name":"Гінандробластома"},"zh":{"name":"两性胚细胞瘤"},"tr":{"name":"Jinandroblastom"}},"xrefs":[{"source":"ICD-10","code":"D39.1","qualifier":"NTBT","icd_relation":"index","validated":true},{"source":"ICD-10","code":"D40.1","qualifier":"NTBT","icd_relation":"index","validated":true},{"source":"ICD-11","code":"2C73.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"278327610"},{"source":"ICD-11","code":"2F96","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1655296936"},{"source":"ICD-11","code":"XH0Q64","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1478416624"},{"source":"MONDO","code":"0020540","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"20540","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0018413","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"9665","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":35808,"name":"Malignant sex cord stromal tumor of ovary","classifications":[202,205]}],"children":[],"genes":[{"symbol":"DICER1","name":"dicer 1, ribonuclease III","gene_type":"gene with protein product","association":"Major susceptibility factor in","status":"Assessed","source":"24761742[PMID]_21205968[PMID]_21882293[PMID]","hgnc":"17098","ensembl":"ENSG00000100697","omim":"606241","loci":["14q32.13"]}],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}