ORPHA:399980
Rare genetic male 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 genetic male infertility | |
| fr | Infertilité masculine rare d'origine génétique | |
| de | Seltene genetisch bedingte Form der männlichen Infertilität | |
| es | Infertilidad masculina rara genética | |
| it | Sterilità maschile genetica rara | |
| nl | Zeldzame genetische mannelijke onvruchtbaarheid | |
| pt | Infertilidade masculina genética rara | |
| pl | Rzadka niepłodność męska uwarunkowana genetycznie | |
| cs | Vzácná geneticky podmíněná mužská neplodnost | |
| uk | Рідкісне генетично обумовлене чоловіче безпліддя | |
| zh | 罕见的遗传性男性不育 | |
| tr | Nadir genetik erkek infertilitesi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18404 | E | validated | |
| UMLS | C5681134 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:275742Genetic infertility
rare genetic diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/399980
- This record as JSON: /data/d/399980.json