ORPHA:400003
Rare genetic disorder with obstructive azoospermia
Synonyms: Rare genetic disorder due to impaired sperm transport
- 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 disorder with obstructive azoospermia | Rare genetic disorder due to impaired sperm transport |
| fr | Maladie génétique rare avec azoospermie obstructive | Maladie génétique rare avec azoospermie excrétoire |
| de | Seltene genetische Störung mit obstruktiver Azoospermie | Seltene genetische Störung durch Beeinträchtigung des Spermientransportes |
| es | Trastorno genético raro con azoospermia obstructiva | Trastorno genético raro por un defecto en el transporte del esperma |
| it | Disturbo genetico raro con azoospermia ostruttiva | Disturbo genetico raro da difetto nel trasporto dello sperma |
| nl | Zeldzame genetische aandoening met obstructieve azoöspermie | Zeldzame genetische aandoening door storing van spermatransport |
| pt | Doença genética rara com azoospermia obstrutiva | |
| pl | Rzadkie genetyczne zaburzenie z azoospermią obstrukcyjną | Rzadkie genetyczne zaburzenie z powodu upośledzonego transportu spermy |
| cs | Vzácné geneticky podmíněné poruchy s obstrukční azoospermií | Vzácné geneticky podmíněné poruchy s porušeným transportem spermií |
| uk | Рідкісне генетично обумовлене захворювання з обструктивною азооспермією | Рідкісне генетичне захворювання, повязане з порушенням транспортування сперматозоїдів |
| zh | 罕见遗传性障碍伴梗阻性无精症 | 精子运输障碍所致罕见遗传性障碍 |
| tr | Obstrüktif azospermi ile seyreden genetik bozukluk | Bozulmuş sperm taşınmasına bağlı nadir görülen genetik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18409 | E | validated | |
| UMLS | C5680007 | 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:399998Male infertility due to obstructive azoospermia of genetic origin
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/400003
- This record as JSON: /data/d/400003.json