Longitudinal vaginal septum
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A rare vaginal malformation characterized by the presence of a complete or incomplete septum dividing the vagina into two parallel cavities, resulting from failure of reabsorption of the midline uterine septum between the two fused Müllerian ducts during embryogenesis. Patients are often asymptomatic, but may present with menorrhagia, dysmenorrhea, dyspareunia, infertility, or spontaneous abortion. The condition may occur as an isolated malformation or in association with other Müllerian duct anomalies (such as septate uterus or uterus didelphys) or renal abnormalities.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Longitudinal vaginal septum | |
| fr | Vagin cloisonné longitudinal | |
| de | Vaginalseptum, longitudinales | |
| es | Septo vaginal longitudinal | |
| it | Setto vaginale longitudinale | |
| nl | Longitudinaal vaginaal septum | |
| pt | Septo vaginal longitudinal | |
| pl | Przegroda podłużna pochwy | |
| cs | Longitudinální poševní septum | |
| uk | Поздовжня перегородка піхви | |
| zh | 阴道纵膈 | |
| tr | Boyuna vajinal septum |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q52.1 | NTBT | attributed | validated |
| ICD-11 | LB42.1 | NTBT | index | validated |
| MONDO | 0015849 | E | validated | |
| UMLS | C1841680 | 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:180154Septate vagina
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/180157
- This record as JSON: /data/d/180157.json