Unicervical bicornuate uterus
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare non-syndromic uterine malformation characterized by a uterus with two uterine horns and only one cervix, resulting from a failure in the fusion of the two Müllerian structures. Depending on the degree of the fusion deficiency, the malformation may be complete with the cavities separated up to the internal orifice of the cervix and not linked, or partial when there is some linkage. Patients may present recurrent pregnancy loss or preterm labor.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Unicervical bicornuate uterus | |
| fr | Uterus bicorne unicervical | |
| de | Uterus bicornis, unizervikaler | |
| es | Útero bicorne unicervical | |
| it | Utero bicorne unicervicale | |
| nl | Unicervicale tweehoornige baarmoeder | |
| pt | Útero bicórneo unicervical | |
| pl | Macica dwurożna jednoszyjkowa | |
| cs | Uterus bicornis unicollis | |
| uk | Дворога матка з одиночною шийкою | |
| zh | 单宫颈双角子宫 | |
| tr | Uniservikal bikornuat uterus |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q51.3 | NTBT | attributed | validated |
| ICD-11 | LB44.3 | NTBT | index | validated |
| MONDO | 0015837 | E | validated | |
| UMLS | C5680490 | 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:180134Bicornuate uterus
rare developmental anomalies during embryogenesis; rare urogenital diseases; 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/180114
- This record as JSON: /data/d/180114.json