ORPHA:180154
Septate vagina
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare vaginal malformation characterized by the presence of a complete or incomplete longitudinal or transverse septum in the vagina due to disrupted fusion or canalization of the solid vaginal plate during embryogenesis. Signs and symptoms depend on the type of septum.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Septate vagina | |
| fr | Vagin cloisonné | |
| de | Vagina, septierte | Vaginalseptum |
| es | Vagina septada | |
| it | Vagina settata | |
| nl | Septum van vagina | Vaginaal septum |
| pt | Vagina septada | |
| pl | Przegroda pochwy | |
| cs | Septovaná vagina | |
| uk | Перегороджена піхва | |
| zh | 有隔阴道 | |
| tr | Septate vajina |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q52.1 | NTBT | inclusion | validated |
| ICD-11 | LB42.1 | E | specific | validated |
| MONDO | 0015848 | E | validated | |
| UMLS | C0266411 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:180151Rare vaginal malformation
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare infertility disorders; rare gynecological and obstetric diseases; rare transplant-related disorders
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180154
- This record as JSON: /data/d/180154.json