ORPHA:180151
Rare vaginal malformation
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare vaginal malformation | |
| fr | Malformation vaginale rare | |
| de | Seltene Fehlbildung der Vagina | |
| es | Malformación vaginal rara | |
| it | Malformazione vaginale rara | |
| nl | Zeldzame vaginale malformatie | |
| pt | Malformação vaginal rara | |
| pl | Rzadka wada pochwy | |
| cs | Vzácné malformace pochvy | |
| uk | Рідкісна вада розвитку піхви | |
| zh | 罕见阴道畸形 | |
| tr | Nadir vajinal malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15847 | E | validated | |
| UMLS | C5680493 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (3):
- ORPHA:182117Non-syndromic urogenital tract malformation of female
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders - ORPHA:98049Rare female infertility
rare infertility disorders - ORPHA:96344Rare gynecologic or obstetric disease
rare gynecological and obstetric diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180151
- This record as JSON: /data/d/180151.json