Complete septate uterus
Synonyms: Total septate uterus
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Complete septate uterus is a rare, non-syndromic uterovaginal malformation characterized by a uterus that has a longitudinal septum which elongates from the uterine fundus to the internal or external cervical os. Most often women are asymptomatic, however dysmenorrhea, unilateral obstruction, and endometriosis could be observed. Unlike urinary tract abnormalities, which are very rarely associated, poor reproductive outcome is frequent.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Complete septate uterus | Total septate uterus |
| fr | Utérus cloisonné total | |
| de | Uterus, komplett septierter | |
| es | Útero septado completo | Útero septado total · Útero tabicado |
| it | Utero settato totale | |
| nl | Baarmoeder met volledig septum | |
| pt | Útero totalmente septado | |
| pl | Macica z przegrodą całkowitą | = en |
| cs | Uterus septus - kompletní | = en |
| uk | Повністю перегороджена матка | Тотальна роздвоєна матка |
| zh | 完全纵膈子宫 | 完全纵膈子宫 |
| tr | Tam septat uterus | Total septat uterus |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q51.2 | NTBT | attributed | validated |
| ICD-11 | LB44.4 | NTBT | index | validated |
| MONDO | 0015840 | E | validated | |
| UMLS | C2957116 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:180122Septate uterus
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare infertility disorders; rare gynecological and obstetric diseases; rare transplant-related disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180126
- This record as JSON: /data/d/180126.json