ORPHA:399771
Male infertility due to sperm 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Male infertility due to sperm disorder | |
| fr | Infertilité masculine due à une anomalie du sperme | |
| de | Männliche Infertilität, Spermien-abhängige | |
| es | Infertilidad masculina por un trastorno del esperma | |
| it | Sterilità maschile da anomalie spermatiche | |
| nl | Mannelijke onvruchtbaarheid door spermastoornis | |
| pt | Infertilidade masculina por alteração do esperma | |
| pl | Niepłodność męska z powodu zaburzeń nasienia | |
| cs | Mužská neplodnost způsobená abnormalitami spermatu | |
| uk | Чоловіче безпліддя, зумовлене порушенням спермограми | |
| zh | 精子异常所致男性不育 | |
| tr | Sperm bozukluğuna bağlı erkek infertilitesi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18390 | E | validated | |
| UMLS | C5681162 | 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:399764Male infertility due to gonadal dysgenesis or sperm disorder
rare genetic diseases; rare infertility disorders
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/399771
- This record as JSON: /data/d/399771.json