ORPHA:180122
Septate uterus
- Type
- Clinical group
- 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 | Septate uterus | |
| fr | Utérus cloisonné | Utérus communiquant |
| de | Uterus Septus | |
| es | Útero septo | |
| it | Utero settato | |
| nl | Septumbaarmoeder | |
| pt | Útero septado | |
| pl | Macica z przegrodą | |
| cs | Uterus septus | |
| uk | Перегороджена матка | |
| zh | 纵膈子宫 | |
| tr | Septate uterus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LB44.4 | E | specific | validated |
| MONDO | 0015839 | E | validated | |
| MONDO | 15839 | E | validated | |
| MeSH | D000093665 | E | validated | |
| UMLS | C0152240 | E | validated | |
| MedDRA | 10062606 | 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 (2):
- ORPHA:180065Non-syndromic uterovaginal malformation
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare gynecological and obstetric diseases; rare transplant-related disorders - ORPHA:399882Rare female infertility due to an implantation defect
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180122
- This record as JSON: /data/d/180122.json