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OHVIRA

medical condition
Class type of: uterine disease, renal agenesis, syndromic urogenital tract malformation Q28439901

Facts

5 properties
Instance of
class of disease
Subclass of
uterine disease, renal agenesis, syndromic urogenital tract malformation, syndromic uterovaginal malformation, rare genetic gynecological and obstetrical diseases, syndromic renal or urinary tract malformation, developmental defect during embryogenesis[6][7][8]
Age of onset
congenital onset, infantile onset, neonatal onset[10][11][12]
Has phenotype
renal agenesis, preterm birth, breech presentation, fever, uterus didelphys, chronic pain, Abnormal uterine cervix morphology, dyspareunia, hydrocolpos, dysmenorrhea, metrorrhagia[13][14][15][16][17][18][19][20][21][22][23]
Prevalence
+0.000001[9]
🏷️ Also known as
en UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS en Wunderlich syndrome en Double uterus and obstructed hemivagina syndrome en Herlyn-Werner syndrome en Herlyn-Werner-Wunderlich syndrome en Obstructed hemivagina and ipsilateral renal anomaly en OHVIRA en OHVIRA syndrome ar متلازمة هرلين-ويرنر-وندرليش de OHVIRA-Syndrom fr Syndrome d'utérus double-hémivagin-agénésie rénale fr Syndrome OHVIRA nl OHVIRA-syndroom pt SHWW pt síndrome de Herlyn–Werner–Wunderlich
🔖 Identifiers · 8
Image (Wikimedia Commons)
OHVIRA Ultrasound.jpg ↗
GARD rare disease ID
1910
MeSH descriptor ID
C566010
Mondo ID
MONDO_0008636
OMIM ID
192050
Orphanet ID
3411
Raras disease ID
D03411
UMLS CUI
C1860549, C4302552

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🔗 Connections
Subclass of 1
renal agenesis
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Summary

OHVIRA is a class of disease[1]. OHVIRA is a type of uterine disease[2], renal agenesis[3], syndromic urogenital tract malformation[4], and syndromic uterovaginal malformation[5].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . Retrieved . wikidata.org.
  22. [23] ↑ . Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). OHVIRA. Retrieved November 8, 2026, from https://4ort.xyz/entity/ohvira
MLA “OHVIRA.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Nov. 2026, https://4ort.xyz/entity/ohvira.
BibTeX @misc{4ortxyz_ohvira_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{OHVIRA}}, year = {2026}, url = {https://4ort.xyz/entity/ohvira}, note = {Accessed: 2026-11-08}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): OHVIRA — https://4ort.xyz/entity/ohvira (retrieved 2026-11-08)

Canonical URL: https://4ort.xyz/entity/ohvira · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 18d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Raras disease ID → D03411
    Prevalence → 0.000001
    Age of onset → congenital onset, infantile onset, neonatal onset
    Has phenotype → renal agenesis, preterm birth, breech presentation +1
    "Changed the item: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Instance of → class of disease
    Subclass of → uterine disease, renal agenesis, syndromic urogenital tract malformation +1
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
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