ORPHA:399831
Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder
Synonyms: Rare female infertility due to gonadotropic axis disorder · Rare female infertility due to hypothalamic-pituitary-ovarian axis disorder
- 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 | Rare female infertility due to gonadotropic axis disorder · Rare female infertility due to hypothalamic-pituitary-ovarian axis disorder |
| fr | Infertilité féminine rare due à un trouble de l'axe hypothalamo-hypophyso-gonadique | Infertilité féminine rare due à un trouble de l'axe gonadotrope · Infertilité féminine rare due à un trouble de l'axe hypothalamo-hypophyso-ovarien |
| de | Seltene Form der weibliche Infertilität durch Störung der Hypothalamus-Hypophysen-Gonaden-Achse | Seltene Form der weibliche Infertilität durch Störung der Hypothalamus-Hypophysen-Ovarien-Achse · Seltene Form der weibliche Infertilität durch Störung der gonadotropen Achse |
| es | Infertilidad femenina rara por un trastorno del eje hipotalámico-hipofisario-gonadal | Infertilidad femenina rara por un trastorno del eje gonadotrópico · Infertilidad femenina rara por un trastorno del eje hipotalámico-hipofisario-testicular |
| it | Sterilità femminile rara da difetto dell'asse ipotalamo-ipofisi-gonadi | Sterilità femminile rara da difetto dell'asse gonadotropo · Sterilità femminile rara da difetto dell'asse ipotalamo-ipofisi-ovaio |
| nl | Zeldzame vrouwelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-gonaden-as | Zeldzame vrouwelijke onvruchtbaarheid door stoornis van gonadotrope as · Zeldzame vrouwelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-ovaria-as |
| pt | Infertilidade feminina rara devido a doença do eixo hipotalâmico-hipofisário-gonadal | |
| pl | Rzadka niepłodność żeńska z powodu zaburzenia osi podwzgórzowo-przysadkowo-gonadalnej | Rzadka niepłodność żeńska z powodu zaburzenia osi gonadotropowej · Rzadka niepłodność żeńska z powodu zaburzenia osi podwzgórzowo-przysadkowo-jajnikowej |
| cs | Vzácná ženská neplodnost způsobená poruchou hypothalamo-hypofyzárně-gonanadální osy | Vzácná ženská neplodnost způsobená poruchou gonadotropní osy · Vzácná ženská neplodnost způsobená poruchou hypothalamo-hypofyzárně-ovariální osy |
| uk | Рідкісне жіноче безпліддя, зумовлене порушенням гіпоталамо-гіпофізарно-гонадної осі | Рідкісне жіноче безпліддя через порушення гонадотропної осі · Рідкісне жіноче безпліддя внаслідок порушення гіпоталамо-гіпофізарно-яєчникової осі |
| zh | 下丘脑-垂体-性腺轴异常导致的罕见女性不育 | 促性腺轴紊乱所致罕见女性不孕 |
| tr | Hipotalamik-hipofiz-gonadal eksen bozukluğuna bağlı nadir kadın infertilitesi | Hipotalamik-hipofiz-yumurtalık aks bozukluğuna bağlı nadir kadın infertilitesi · Gonadotropik aks bozukluğuna bağlı nadir kadın infertilitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18397 | E | validated | |
| UMLS | C5680030 | 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:98049Rare female infertility
rare infertility disorders
Children (8):
- ORPHA:963Acromegaly
- ORPHA:91Aromatase deficiency
- ORPHA:785Estrogen resistance syndrome
- ORPHA:397685Familial hyperprolactinemia
- ORPHA:2965Prolactinoma
- ORPHA:399839Rare female infertility due to a congenital hypogonadotropic hypogonadism
- ORPHA:399849Rare female infertility due to an adrenal disorder
- ORPHA:399853Rare female infertility due to an anomaly of ovarian function
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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/399831
- This record as JSON: /data/d/399831.json