{"orpha":399846,"name":"Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism","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-399846/","orphanet_url":"https://www.orpha.net/en/disease/detail/399846","names":{"fr":{"name":"Maladie rare avec Infertilité féminine due à un hypogonadisme hypogonadotrope congénital"},"de":{"name":"Seltene Störung mit weiblicher Infertilität durch kongenitalen hypogonadotropen Hypogonadismus"},"es":{"name":"Trastorno raro con infertilidad femenina por hipogonadismo hipogonadotrópico congénito"},"it":{"name":"Disturbo raro con sterilità femminile da ipogonadismo ipogonadotropo congenito"},"nl":{"name":"Zeldzame aandoening met vrouwelijke onvruchtbaarheid door congenitaal hypogonadotroop hypogonadisme"},"pt":{"name":"Doença rara com infertilidade feminina devido a hipogonadismo hipogonadotrópico congénito"},"pl":{"name":"Rzadkie zaburzenie z niepłodnością żeńską z powodu wrodzonego hipogonadyzmu hipogonadotropowego"},"cs":{"name":"Vzácná porucha doprovázená ženskou neplodností, způsobená vrozeným hypogonadotropním hypogonadismem"},"uk":{"name":"Рідкісне захворювання з жіночим безпліддям, зумовленим вродженим гіпогонадотропним гіпогонадизмом"},"zh":{"name":"Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism"},"tr":{"name":"Doğumsal hipogonadotropik hipogonadizme bağlı kadın infertilitesi ile seyreden nadir bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681161","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":399839,"name":"Rare female infertility due to a congenital hypogonadotropic hypogonadism","classifications":[156,201]}],"children":[{"orpha":110,"name":"Bardet-Biedl syndrome","type":"Disease"},{"orpha":138,"name":"CHARGE syndrome","type":"Malformation syndrome"},{"orpha":739,"name":"Prader-Willi syndrome","type":"Disease"},{"orpha":398073,"name":"Prader-Willi-like syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}