{"orpha":181441,"name":"Rare disorder with hypergonadotropic hypogonadism","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare disorder with primary hypogonadism"],"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-181441/","orphanet_url":"https://www.orpha.net/en/disease/detail/181441","names":{"fr":{"name":"Maladie rare avec hypogonadisme hypergonadotrope","synonyms":["Maladie rare avec hypogonadisme primaire"]},"de":{"name":"Seltene Syndrome mit hypergonadotropen Hypogonadismus","synonyms":["Seltene Störung mit primärem Hypogonadismus"]},"es":{"name":"Enfermedad rara con hipogonadismo hipergonadotrópico","synonyms":["Enfermedad rara con hipogonadismo primario"]},"it":{"name":"Disturbo raro con ipogonadismo ipergonadotropo","synonyms":["Disturbo raro con ipogonadismo primitivo"]},"nl":{"name":"Zeldzame stoornis met hypergonadotroop hypogonadisme","synonyms":["Zeldzame stoornis met primair hypogonadisme"]},"pt":{"name":"Doença rara com hipogonadismo hipergonadotrópico","synonyms":["Doença rara com hipogonadismo primário"]},"pl":{"name":"Rzadka choroba z hipogonadyzmem hipergonadotropowym","synonyms":["Rzadka choroba z hipogonadyzmem pierwotnym"]},"cs":{"name":"Vzácná onemocnění s hypergonadotropním hypogonadismem","synonyms":["Vzácná onemocnění s primárním hypogonadismem"]},"uk":{"name":"Рідкісний розлад з гіпергонадотропним гіпогонадизмом","synonyms":["Рідкісний розлад з первинним гіпогонадизмом"]},"zh":{"name":"罕见病伴性腺功能减退症","synonyms":["伴原发性性腺机能减退的罕见病"]},"tr":{"name":"Hipergonadotropik hipogonadizm ile seyreden nadir bozukluk","synonyms":["Primer hipogonadizm ile nadir bozukluk"]}},"xrefs":[{"source":"MONDO","code":"15906","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679596","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":97978,"name":"Rare endocrine disease","classifications":[193]},{"orpha":156638,"name":"Rare genetic endocrine disease","classifications":[156]},{"orpha":399685,"name":"Rare male infertility due to testicular endocrine disorder","classifications":[156,201]}],"children":[{"orpha":90646,"name":"Deafness-hypogonadism syndrome","type":"Malformation syndrome"},{"orpha":2229,"name":"Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","type":"Malformation syndrome"},{"orpha":2183,"name":"Hydrocephalus-obesity-hypogonadism syndrome","type":"Malformation syndrome"},{"orpha":2410,"name":"Hypergonadotropic hypogonadism-cataract syndrome","type":"Malformation syndrome"},{"orpha":2233,"name":"Hypogonadism-mitral valve prolapse-intellectual disability syndrome","type":"Disease"},{"orpha":3044,"name":"Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome","type":"Malformation syndrome"},{"orpha":2234,"name":"Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome","type":"Malformation syndrome"},{"orpha":2558,"name":"Mikati-Najjar-Sahli syndrome","type":"Malformation syndrome"},{"orpha":280679,"name":"Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome","type":"Disease"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":2232,"name":"Primary hypergonadotropic hypogonadism-partial alopecia syndrome","type":"Disease"},{"orpha":606,"name":"Proximal myotonic myopathy","type":"Disease"},{"orpha":3464,"name":"Woodhouse-Sakati syndrome","type":"Disease"},{"orpha":43,"name":"X-linked adrenoleukodystrophy","type":"Disease"},{"orpha":163971,"name":"X-linked intellectual disability, Cilliers type","type":"Disease"},{"orpha":163976,"name":"X-linked intellectual disability, Van Esch type","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}