{"orpha":399853,"name":"Rare female infertility due to an anomaly of ovarian function","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-399853/","orphanet_url":"https://www.orpha.net/en/disease/detail/399853","names":{"fr":{"name":"Infertilité féminine rare due à un dysfonctionnement ovarien"},"de":{"name":"Seltene Form der weibliche Infertilität durch Funktionsanomalie des Ovars"},"es":{"name":"Infertilidad femenina rara por una anomalía de la función ovárica"},"it":{"name":"Sterilità femminile rara da difetto della funzione ovarica"},"nl":{"name":"Zeldzame vrouwelijke onvruchtbaarheid door functiestoornis van ovarium"},"pt":{"name":"Infertilidade feminina rara por anomalia da função ovárica"},"pl":{"name":"Rzadka niepłodność żeńska z powodu nieprawidłowego funkcjonowania jajników"},"cs":{"name":"Vzácná ženská neplodnost způsobená anomáliemi ovariálních funkcí"},"uk":{"name":"Рідкісне жіноче безпліддя, зумовлене аномалією функції яєчників"},"zh":{"name":"卵巢功能异常所致罕见女性不育"},"tr":{"name":"Yumurtalık fonksiyonunun anormalliğine bağlı nadir kadın infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18401","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681159","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":399831,"name":"Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder","classifications":[201]}],"children":[{"orpha":3453,"name":"Autoimmune polyendocrinopathy type 1","type":"Disease"},{"orpha":3143,"name":"Autoimmune polyendocrinopathy type 2","type":"Disease"},{"orpha":572354,"name":"Blepharophimosis-ptosis-epicanthus inversus syndrome type 1","type":"Clinical subtype"},{"orpha":79239,"name":"Classic galactosemia","type":"Disease"},{"orpha":2297,"name":"Insulin-resistance syndrome type A","type":"Disease"},{"orpha":75325,"name":"Osteosclerosis-ichthyosis-premature ovarian failure syndrome","type":"Disease"},{"orpha":9,"name":"Tetrasomy X syndrome","type":"Malformation syndrome"},{"orpha":3375,"name":"Trisomy X syndrome","type":"Malformation syndrome"},{"orpha":96201,"name":"X small rings syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}