ORPHA:400018
Rare female infertility due to adrenal 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare female infertility due to adrenal disorder of genetic origin | |
| fr | Infertilité féminine rare due à une anomalie surrénalienne d'origine génétique | Infertilité féminine rare due à une anomalie des surrénales d'origine génétique |
| de | Seltene Form der weibliche Infertilität durch genetisch bedingter Nebennierenstörung | |
| es | Infertilidad femenina rara por un trastorno suprarrenal de origen genético | |
| it | Sterilità femminile rara da disturbo ipofisario di origine genetica | |
| nl | Zeldzame vrouwelijke infertiliteit door aandoening van bijnier van genetische oorsprong | Zeldzame vrouwelijke onvruchtbaarheid door adrenale stoornis van genetische oorsprong |
| pt | Infertilidade feminina rara por doença supra-renal de origem genética | |
| pl | Rzadka niepłodność żeńska z powodu zaburzeń nadnerczy pochodzenia genetycznego | |
| cs | Vzácná ženská neplodnost způsobená poruchou nadledvin genetického původu | |
| uk | Рідкісне жіноче безпліддя, зумовлене генетично обумовленим захворюванням надниркових залоз | |
| zh | 遗传性肾上腺疾病导致的罕见女性不育 | |
| tr | Genetik kökenli adrenal bozukluğa bağlı nadir kadın infertilitesi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18412 | E | validated | |
| UMLS | C5681138 | 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):
Children (4):
- ORPHA:75246,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- ORPHA:90794Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- ORPHA:90793Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
- ORPHA:90790Congenital lipoid adrenal hyperplasia due to STAR deficency
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/400018
- This record as JSON: /data/d/400018.json