{"orpha":174590,"name":"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-174590/","orphanet_url":"https://www.orpha.net/en/disease/detail/174590","names":{"fr":{"name":"Hypogonadisme hypogonadotrope congénital"},"de":{"name":"Hypogonadotroper Hypogonadismus, kongenitaler"},"es":{"name":"Hipogonadismo hipogonadotrópico congénito"},"it":{"name":"Ipogonadismo ipogonadotropo congenito"},"nl":{"name":"Congenitaal hypogonadotroop hypogonadisme"},"pt":{"name":"Hipogonadismo hipogonadotrópico congénito"},"pl":{"name":"Wrodzony hipogonadyzm hipogonadotropowy"},"cs":{"name":"Vrozený hypogonadotropní hypogonadismus"},"uk":{"name":"Вроджений гіпогонадотропний гіпогонадизм"},"zh":{"name":"先天性低促性腺激素性性腺功能减退症"},"tr":{"name":"Doğumsal hipogonadotropik hipogonadizm"}},"xrefs":[{"source":"MONDO","code":"0015770","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15770","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C3899503","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10083932","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":180208,"name":"Anomaly of puberty or/and menstrual cycle","classifications":[205]},{"orpha":202940,"name":"Anomaly of puberty or/and menstrual cycle of genetic origin","classifications":[156]},{"orpha":95488,"name":"Non-acquired pituitary hormone deficiency","classifications":[156,193]},{"orpha":399572,"name":"Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder","classifications":[201]},{"orpha":399983,"name":"Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin","classifications":[156]}],"children":[{"orpha":181390,"name":"Endocrinopathy with congenital hypogonadotropic hypogonadism as a major feature","type":"Category"},{"orpha":238666,"name":"Isolated congenital hypogonadotropic hypogonadism","type":"Disease"},{"orpha":52901,"name":"Isolated follicle stimulating hormone deficiency","type":"Disease"},{"orpha":181387,"name":"Rare disorder with multisystemic involvement and congenital hypogonadotropic hypogonadism","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant","Autosomal recessive","X-linked recessive"],"onset":["Infancy","Neonatal"],"prevalence":[],"phenotypes":null}