Partial septate uterus
Synonyms: Subtotal septate uterus · Uterus subseptus
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Partial septate uterus is a rare, non-syndromic uterovaginal malformation characterized by a uterus that has a longitudinal septum which extends from the uterine fundus and does not reach the internal cervical os (variable lengths and widths may be observed). Although frequently asymptomatic, an increased risk of poor reproductive outcome has been observed. Urinary tract abnormalities are very rarely associated.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Partial septate uterus | Subtotal septate uterus · Uterus subseptus |
| fr | Utérus cloisonné subtotal | Utérus subseptus |
| de | Uterus, teilseptierter | |
| es | Útero septado parcial | Útero septado subtotal · Útero subseptado · Útero subtabicado |
| it | Utero settato subtotale | |
| nl | Baarmoeder met onvolledig septum | uterus subseptus |
| pt | Útero subseptado | |
| pl | Macica z przegrodą częściową | = en |
| cs | Uterus subseptus | = en |
| uk | Частково перегороджена матка | Субтотальна септована матка · Підсегмент матки |
| zh | 不完全纵膈子宫 | 不完全纵膈子宫 |
| tr | Kısmi septat uterus | Uterus subeptus · Subtotal septate 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 | 0015841 | E | validated | |
| UMLS | C0266401 | 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/180129
- This record as JSON: /data/d/180129.json