{"orpha":101433,"name":"Rare urogenital disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-101433/","orphanet_url":"https://www.orpha.net/en/disease/detail/101433","names":{"fr":{"name":"Maladie urogénitale rare"},"de":{"name":"Urogenitale Krankheit, seltene"},"es":{"name":"Enfermedad urogenital rara"},"it":{"name":"Malattia genitourinaria rara"},"nl":{"name":"Zeldzame urogenitale ziekte"},"pt":{"name":"Doença urogenital rara"},"pl":{"name":"Rzadkie choroby moczowo-płciowe"},"cs":{"name":"Vzácné urogenitální onemocnění"},"uk":{"name":"Рідкісне сечостатеве захворювання"},"zh":{"name":"罕见泌尿生殖系统疾病"},"tr":{"name":"Nadir ürogenital hastalık"}},"xrefs":[{"source":"MONDO","code":"15106","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681790","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":90771,"name":"Difference of sex development","type":"Category"},{"orpha":708684,"name":"Eosinophilic cystitis","type":"Disease"},{"orpha":2795,"name":"Fowler urethral sphincter dysfunction syndrome","type":"Disease"},{"orpha":84085,"name":"Hinman syndrome","type":"Disease"},{"orpha":37202,"name":"Interstitial cystitis","type":"Disease"},{"orpha":692256,"name":"Isolated anogenital granulomatosis","type":"Disease"},{"orpha":140949,"name":"Low-flow priapism","type":"Particular clinical situation in a disease or syndrome"},{"orpha":404463,"name":"Multisystemic smooth muscle dysfunction syndrome","type":"Disease"},{"orpha":182114,"name":"Rare urogenital tumor","type":"Category"},{"orpha":693872,"name":"Urinary tract arteriovenous malformation","type":"Malformation syndrome"},{"orpha":83001,"name":"Urogenital tract malformation","type":"Category"},{"orpha":693815,"name":"Uterine arteriovenous malformation","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}