Transverse vaginal septum
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A rare vaginal malformation characterized by the presence of a complete or incomplete transverse septum at any level of the vagina (most frequently the upper or middle third), resulting from incomplete fusion between the Müllerian duct component and the urogenital sinus component of the vagina during embryogenesis. The condition is only rarely diagnosed in neonates or infants, unless it causes significant hydromucocolpos. Complete septa present with primary amenorrhea, cyclic pelvic pain, dyspareunia, or a pelvic mass consisting of accumulated menstrual blood, while incomplete septa may lead to dyspareunia and dysmenorrhea.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Transverse vaginal septum | |
| fr | Vagin cloisonné transversal | Diaphragme vaginal |
| de | Vaginalseptum, transversales | |
| es | Septo vaginal transverso | |
| it | Setto vaginale trasversale | |
| nl | Dwars vaginaal septum | |
| pt | Septo vaginal transverso | |
| pl | Przegroda poprzeczna pochwy | |
| cs | Transverzální poševní septum | |
| uk | Поперечна перегородка піхви | |
| zh | 阴道横膈 | |
| tr | Enine 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 | 0015850 | E | validated | |
| UMLS | C1856006 | 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/180160
- This record as JSON: /data/d/180160.json