ORPHA:400011
Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
Synonyms: Rare female infertility due to gonadotropic axis disorder of genetic origin · Rare female infertility due to hypothalamic-pituitary-testicular axis disorder of genetic origin
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin | Rare female infertility due to gonadotropic axis disorder of genetic origin · Rare female infertility due to hypothalamic-pituitary-testicular axis disorder of genetic origin |
| fr | Infertilité féminine rare due à un trouble de l'axe hypothalamo-hypophyso-gonadique d'origine génétique | Infertilité féminine rare due à un trouble de l'axe gonadotrope d'origine génétique · Infertilité féminine rare due à un trouble de l'axe hypothalamo-hypophyso-testiculaire d'origine génétique |
| de | Seltene Form der weibliche Infertilität durch genetische Störung der Hypothalamus-Hypophysen-Gonaden-Achse | Seltene Form der weibliche Infertilität durch genetische Störung der Hypothalamus-Hypophysen-Ovarien-Achse · Seltene Form der weibliche Infertilität durch genetische Störung der gonadotropen Achse |
| es | Infertilidad femenina rara por un trastorno del eje hipotalámico-hipofisario-gonadal de origen genético | Infertilidad femenina rara por un trastorno del eje gonadotrópico de origen genético · Infertilidad femenina rara por un trastorno del eje hipotalámico-hipofisario-testicular de origen genético |
| it | Sterilità femminile rara da difetto dell'asse ipotalamo-ipofisi-gonadi di origine genetica | Sterilità femminile rara da difetto dell'asse gonadotropo di origine genetica · Sterilità femminile rara da difetto dell'asse ipotalamo-ipofisi-ovaio di origine genetica |
| nl | Zeldzame vrouwelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-gonaden-as van genetische oorsprong | Zeldzame vrouwelijke onvruchtbaarheid door stoornis van gonadotrope as van genetische oorsprong · Zeldzame vrouwelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-ovaria-as van genetische oorsprong |
| pt | Infertilidade feminina rara por alteração do eixo hipotálamo-hipófise-gonadal de origem genética | |
| pl | Rzadka niepłodność żeńska z powodu zaburzeń osi podwzgórzowo-przysadkowo-gonadalnej pochodzenia genetycznego | Rzadka niepłodność żeńska z powodu zaburzeń osi gonadotropowej pochodzenia genetycznego · Rzadka niepłodność żeńska z powodu zaburzeń osi podwzgórzowo-przysadkowo-jajnikowej pochodzenia genetycznego |
| cs | Vzácná ženská neplodnost způsobená poruchou hypothalamo-hypofyzárně-gonadální osy genetického původu | Vzácná ženská neplodnost způsobená poruchou gonadotropní osy genetického původu · Vzácná ženská neplodnost způsobená poruchou hypothalamo-hypofyzárně-testikulární osy genetického původu |
| uk | Рідкісне жіноче безпліддя, зумовлене генетично обумовленим порушенням гіпоталамо-гіпофізарно-гонадної осі | Рідкісне жіноче безпліддя через порушення гонадотропної осі генетичного походження · Рідкісне жіноче безпліддя через порушення гіпоталамо-гіпофізарно-тестикулярної осі генетичного походження |
| zh | 遗传性下丘脑-垂体-性腺轴障碍导致的罕见女性不育 | 遗传性下丘脑-垂体-睾丸轴紊乱所致罕见女性不孕 |
| tr | Genetik kökenli hipotalamik-hipofiz-gonadal eksen bozukluğuna bağlı nadir kadın infertilitesi | Genetik kaynaklı gonadotropik aks bozukluğuna bağlı nadir kadın infertilitesi · Genetik kaynaklı hipotalamik-hipofiz-testis eksen bozukluğuna bağlı nadir kadın infertilitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18411 | E | validated | |
| UMLS | C5680011 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:400008Rare genetic female infertility
rare genetic diseases
Children (7):
- ORPHA:91Aromatase deficiency
- ORPHA:785Estrogen resistance syndrome
- ORPHA:397685Familial hyperprolactinemia
- ORPHA:52901Isolated follicle stimulating hormone deficiency
- ORPHA:399839Rare female infertility due to a congenital hypogonadotropic hypogonadism
- ORPHA:400018Rare female infertility due to adrenal disorder of genetic origin
- ORPHA:400022Rare female infertility due to an anomaly of ovarian function of genetic origin
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/400011
- This record as JSON: /data/d/400011.json