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penoscrotal transposition

Congenital variation of genital configuration
Class type of: non-syndromic urogenital tract malformation of male, transposition, developmental defect during embryogenesis Q55786963

Facts

5 properties
Instance of
class of disease, intersex condition[5]
Subclass of
non-syndromic urogenital tract malformation of male, transposition, developmental defect during embryogenesis
Age of onset
infantile onset, neonatal onset[7][8]
Has phenotype
hypospadias, renal agenesis, renal hypodysplasia, micrognathism, pectus carinatum, cardiomyopathy, penoscrotal transposition, shawl scrotum, Wikidata item[9][10][11][12][13][14][15][16][17]
NCI Thesaurus ID
C99010[6]
🏷️ Also known as
en Congenital Penoscrotal Transposition en penoscrotal transposition ar تغيير وضع قضيبي صفني ar تغير مواضيع القضيب والصفن ar تغيير الوضع القضيبي الصفني fr transposition péno-scrotale fr transposition pénoscrotale ja 陰茎前位陰囊 ja 陰茎陰嚢転位
🔖 Identifiers · 12
Exact match
purl.obolibrary.org, www.orpha.net
GARD rare disease ID
4273
Homosaurus ID (V3)
homoit0002870
Homosaurus ID (V4)
homoit0002870
Human Phenotype Ontology ID
HP:0100600
ICD-10-CM
Q55.8
MeSH descriptor ID
C536650
Miraheze article ID
lgbta:Penoscrotal_Transposition
Mondo ID
MONDO_0017285
Orphanet ID
2842
Raras disease ID
D02842
UMLS CUI
C1868854

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Summary

penoscrotal transposition is a class of disease[1]. It is a type of non-syndromic urogenital tract malformation of male[2], transposition[3], and developmental defect during embryogenesis[4].

References

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

Direct Wikidata claims

  1. [5] ↑ . wikidata.org.
  2. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [3] ↑ . wikidata.org.
  4. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . 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.

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). penoscrotal transposition. Retrieved November 7, 2026, from https://4ort.xyz/entity/penoscrotal-transposition
MLA “penoscrotal transposition.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/penoscrotal-transposition.
BibTeX @misc{4ortxyz_penoscrotal-transposition_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{penoscrotal transposition}}, year = {2026}, url = {https://4ort.xyz/entity/penoscrotal-transposition}, note = {Accessed: 2026-11-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): penoscrotal transposition — https://4ort.xyz/entity/penoscrotal-transposition (retrieved 2026-11-07)

Canonical URL: https://4ort.xyz/entity/penoscrotal-transposition · 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. 16d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Age of onset → infantile onset, neonatal onset
    Has phenotype → hypospadias, renal agenesis, renal hypodysplasia +6
    Raras disease ID → D02842
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo ID → MONDO_0017285
    GARD rare disease ID → 4273
    Orphanet ID → 2842
    Instance of → class of disease, intersex condition
    + 11 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.