{"orpha":181390,"name":"Endocrinopathy with congenital hypogonadotropic hypogonadism as a major feature","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-181390/","orphanet_url":"https://www.orpha.net/en/disease/detail/181390","names":{"fr":{"name":"Endocrinopathie avec hypogonadisme hypogonadotrope congénital comme manifestation majeure"},"de":{"name":"Endokrinopathie mit kongenitalen hypogonadotropen Hypogonadismus als Hauptmerkmal"},"es":{"name":"Endocrinopatía con hipogonadismo hipogonadotrópico congénito como característica principal"},"it":{"name":"Ipogonadismo ipogonadotropo associato ad altre endocrinopatie"},"nl":{"name":"Endocrinopathie met congenitaal hypogonadotroop hypogonadisme als hoofdkenmerk"},"pt":{"name":"Endocrinopatia com hipogonadismo hipogondatrópico como característica principal"},"pl":{"name":"Hipogonadyzm hipogonadotropowy związany z innymi endokrynopatiami"},"cs":{"name":"Hypogonadotropní hypogonadismus asociovaný s jinými endokrinopatiemi"},"uk":{"name":"Ендокринопатія з вродженим гіпогонадотропним гіпогонадизмом як основною ознакою"},"zh":{"name":"促性腺素性功能减退症伴其他内分泌疾病"},"tr":{"name":"Diğer endokrinopatilerle -ilişkili hipogonadotropik hipogonadizm"}},"xrefs":[{"source":"MONDO","code":"15891","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680475","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":174590,"name":"Congenital hypogonadotropic hypogonadism","classifications":[156,193,201,205]},{"orpha":399839,"name":"Rare female infertility due to a congenital hypogonadotropic hypogonadism","classifications":[156,201]}],"children":[{"orpha":95494,"name":"Combined pituitary hormone deficiencies, genetic forms","type":"Disease"},{"orpha":95700,"name":"Familial adrenal hypoplasia with absent pituitary luteinizing hormone","type":"Disease"},{"orpha":90695,"name":"Non-acquired panhypopituitarism","type":"Disease"},{"orpha":66628,"name":"Obesity due to congenital leptin deficiency","type":"Etiological subtype"},{"orpha":179494,"name":"Obesity due to leptin receptor gene deficiency","type":"Etiological subtype"},{"orpha":71528,"name":"Obesity due to prohormone convertase I deficiency","type":"Etiological subtype"},{"orpha":95702,"name":"X-linked adrenal hypoplasia congenita","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}