{"orpha":400022,"name":"Rare female infertility due to an anomaly of ovarian function 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-400022/","orphanet_url":"https://www.orpha.net/en/disease/detail/400022","names":{"fr":{"name":"Infertilité féminine rare due à un dysfonctionnement ovarien d'origine génétique"},"de":{"name":"Seltene Form der weibliche Infertilität durch genetisch bedingte Funktionsstörung der Ovarien"},"es":{"name":"Infertilidad femenina rara por una anomalía de la función ovárica de origen genético"},"it":{"name":"Sterilità femminile rara da difetto della funzione ovarica di origine genetica"},"nl":{"name":"Zeldzame vrouwelijke onvruchtbaarheid door functiestoornis van ovarium van genetische oorsprong"},"pt":{"name":"Infertilidade feminina rara por anomalia da função ovariana de origem genética"},"pl":{"name":"Rzadka niepłodność żeńska z powodu nieprawidłowej funkcji jajników pochodzenia genetycznego"},"cs":{"name":"Vzácná ženská neplodnost způsobená anomáliemi ovariální funkce genetického původu"},"uk":{"name":"Рідкісне жіноче безпліддя, зумовлене генетично обумовленою аномалією функції яєчників"},"zh":{"name":"遗传性卵巢功能异常导致的罕见女性不孕"},"tr":{"name":"Genetik kökenli yumurtalık fonksiyonunun anomalisine bağlı nadir kadın infertilitesi"}},"xrefs":[{"source":"MONDO","code":"18413","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681137","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":400011,"name":"Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin","classifications":[156]}],"children":[{"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}