Home › Entities › genetic nervous system disorder › dipygus

dipygus

severe congenital deformity where the body axis forks left and right partway along the torso with the pelvis and legs duplicated
Class type of: genetic nervous system disorder, other syndrome with a central nervous system malformation as major feature, syndromic anorectal malformation Q5280135

Facts

6 properties
Instance of
rare disease, class of disease[6]
Subclass of
genetic nervous system disorder, other syndrome with a central nervous system malformation as major feature, syndromic anorectal malformation, Caudal duplication, developmental defect during embryogenesis[7]
Age of onset
congenital onset, neonatal onset[9][10]
Genetic association
AXIN1[8]
Has phenotype
spina bifida, myelomeningocele, uterus didelphys, Spinal cord lesion, cryptorchidism, omphalocele, urogenital fistula[11][12][13][14][15][16][17]
P14914
D01756[18]
🏷️ Also known as
en caudal duplication en Caudal Duplication Anomaly en dipygus en Split notochord syndrome ar مزدوج الحوض fa دیپیگس fr Dipygus fr Syndrome de la chorde dorsale fendue pt Dípigo zh 双臀畸胎
🔖 Identifiers · 12
Image (Wikimedia Commons)
Myrtle Corbin.jpg ↗
Exact match
www.orpha.net
GARD rare disease ID
1164
ICD-10-CM
Q87.8
KEGG ID
H00934
MeSH descriptor ID
C564315
Microsoft Academic ID (discontinued)
2780862463
Mondo ID
MONDO_0011928
OMIM ID
607864
Orphanet ID
1756
UMLS CUI
C0544738, C1842884, C0266688
UniProt disease ID
DI-02877

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Genetic association 1
AXIN1
Instance of 1
rare disease
← Genetic association 1
AXIN1
← Medical condition 1
Myrtle Corbin
Press Enter · cited answer in seconds

Summary

dipygus is a rare disease[1]. dipygus is a type of genetic nervous system disorder[2], other syndrome with a central nervous system malformation as major feature[3], syndromic anorectal malformation[4], and Caudal duplication[5].

References

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

Direct Wikidata claims

  1. [6] ↑ . wikidata.org.
  2. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [5] ↑ . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . UniProt. 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] ↑ . 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). dipygus. Retrieved November 1, 2026, from https://4ort.xyz/entity/dipygus
MLA “dipygus.” 4ort.xyz Knowledge Graph, 4ort.xyz, 1 Nov. 2026, https://4ort.xyz/entity/dipygus.
BibTeX @misc{4ortxyz_dipygus_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dipygus}}, year = {2026}, url = {https://4ort.xyz/entity/dipygus}, note = {Accessed: 2026-11-01}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): dipygus — https://4ort.xyz/entity/dipygus (retrieved 2026-11-01)

Canonical URL: https://4ort.xyz/entity/dipygus · 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. 12d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'en', 'fa', 'fr', 'pt', 'sr']
    Age of onset → congenital onset, neonatal onset
    Has phenotype → spina bifida, myelomeningocele, uterus didelphys +4
    P14914 → D01756
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 17w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Genetic association → AXIN1
    Subclass of → —
    Instance of → rare disease, class of disease
    Instance of → —
    + 2 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.