ORPHA:180065
Non-syndromic uterovaginal 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic uterovaginal malformation | |
| fr | Malformation utérovaginale non syndromique | |
| de | Uterovaginale Fehlbildung, nicht-syndromale | |
| es | Malformación uterovaginal no sindrómica | |
| it | Malformazione uterovaginale non sindromica | |
| nl | Niet-syndromale uterovaginale malformatie | |
| pt | Malformação uterovaginal não-sindromática | |
| pl | Niesyndromiczna wada macicy i pochwy | |
| cs | Nesyndromické malformace dělohy a pochvy | |
| uk | Несиндромальна матково-вагінальна вада розвитку | |
| zh | 非综合征性子宫阴道畸形 | |
| tr | Sendromik olmayan uterovajinal malformasyon |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15829 | E | validated | |
| UMLS | C5680487 | 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 (2):
- ORPHA:182117Non-syndromic urogenital tract malformation of female
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders - ORPHA:180062Uterovaginal malformation
rare gynecological and obstetric diseases
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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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180065
- This record as JSON: /data/d/180065.json