ORPHA:98049
Rare female infertility
- 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 | |
| fr | Infertilité féminine rare | |
| de | Infertilität, weibliche, seltene | |
| es | Infertilidad femenina rara | |
| it | Sterilità femminile rara | |
| nl | Zeldzame vrouwelijke onvruchtbaarheid | |
| pt | Infertilidade feminina rara | |
| pl | Rzadka niepłodność żeńska | |
| cs | Vzácná ženská neplodnost | |
| uk | Рідкісне жіноче безпліддя | |
| zh | 罕见女性不孕症 | |
| tr | Nadir kadın kısırlığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681512 | 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:98047Rare infertility
rare infertility disorders
Children (5):
- ORPHA:399882Rare female infertility due to an implantation defect
- ORPHA:399877Rare female infertility due to gonadal dysgenesis
- ORPHA:399831Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder
- ORPHA:404469Rare female infertility due to oocyte maturation defect
- ORPHA:180151Rare vaginal malformation
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/98049
- This record as JSON: /data/d/98049.json