ORPHA:399572
Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder
Synonyms: Rare male infertility due to gonadotropic axis disorder · Rare male infertility due to hypothalamic-pituitary-testicular 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 male infertility due to hypothalamic-pituitary-gonadal axis disorder | Rare male infertility due to gonadotropic axis disorder · Rare male infertility due to hypothalamic-pituitary-testicular axis disorder |
| fr | Infertilité masculine rare due à un trouble de l'axe hypothalamo-hypophyso-gonadique | Infertilité masculine rare due à un trouble de l'axe gonadotrope · Infertilité masculine rare due à un trouble de l'axe hypothalamo-hypophyso-testiculaire |
| de | Seltene Form der männlichen Infertilität durch Störung der Hypothalamus-Hypophysen-Gonaden-Achse | Seltene Form der männlichen Infertilität durch Störung der Hypothalamus-Hypophysen-Testes Achse · Seltene Form der männlichen Infertilität durch Störung der gonadotropen Achse |
| es | Infertilidad masculina rara por un trastorno del eje hipotalámico-hipofisario-gonadal | Infertilidad masculina rara por un trastorno del eje gonadotrópico · Infertilidad masculina rara por un trastorno del eje hipotalámico-hipofisario-testicular |
| it | Sterilità maschile rara da difetto dell'asse ipotalamo-ipofisi-gonadi | Sterilità maschile rara da difetto dell'asse gonadotropo · Sterilità maschile rara da difetto dell'asse ipotalamo-ipofisi-testicolo |
| nl | Zeldzame mannelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-gonaden-as | Zeldzame mannelijke onvruchtbaarheid door stoornis van gonadotrope as · Zeldzame mannelijke onvruchtbaarheid door stoornis van hypothalamus-hypofyse-testes-as |
| pt | Infertilidade masculina rara devida a doença do eixo hipotalâmico-hipofisário-gonadal | Infertilidade masculina rara por doença do eixo gonadotrópico · Infertilidade masculina rara por doença do eixo hipotalâmico-hipofisário-testicular |
| pl | Rzadka niepłodność męska z powodu zaburzenia osi podwzgórzowo-przysadkowo-gonadalnej | Rzadka niepłodność męska z powodu zaburzenia osi gonadotropowej · Rzadka niepłodność męska z powodu zaburzenia osi podwzgórzowo-przysadkowo-jądrowej |
| cs | Vzácná mužská neplodnost způsobená poruchou hypothalamo-hypofyzárně-gonadální osy | Vzácná mužská neplodnost způsobená poruchou gonadotropní osy · Vzácná mužská neplodnost způsobená poruchou hypothalamo-hypofyzárně-testikulární osy |
| uk | Рідкісне чоловіче безпліддя, зумовлене порушенням гіпоталамо-гіпофізарно-гонадної осі | Рідкісне чоловіче безпліддя через порушення гонадотропної осі · Рідкісне чоловіче безпліддя через порушення гіпоталамо-гіпофізарно-тестикулярної осі |
| zh | 下丘脑-垂体-性腺轴异常所致罕见男性不育 | 因促性腺激素轴紊乱所致罕见男性不育 |
| tr | Hipotalamik-hipofiz-gonadal eksen bozukluğuna bağlı nadir erkek infertilitesi | Hipotalamik-hipofiz-testis eksen bozukluğuna bağlı nadir erkek infertilitesi · Gonadotropik eksen bozukluğuna bağlı nadir erkek infertilitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18386 | E | validated | |
| UMLS | C5680034 | 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:98048Rare male infertility
rare infertility disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98310OBSOLETE: Male infertility with impaired virilization due to an hypothalamic or pituitary disorder referred to · inactive
- ORPHA:98329OBSOLETE: Male infertility with normal virilization due to a hypothalamic or pituitary defect referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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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/399572
- This record as JSON: /data/d/399572.json