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synpolydactyly

syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene
Class type of: syndactyly, polydactyly, dysostosis of genetic origin with limb anomaly as a major feature Q7662637

Facts

7 properties
Instance of
rare disease, class of disease[6]
Subclass of
syndactyly, polydactyly, dysostosis of genetic origin with limb anomaly as a major feature, developmental defect during embryogenesis
Genetic association
FBLN1, HOXD13[9][10]
Has phenotype
preaxial Hallucal polydactyly[12]
NCI Thesaurus ID
C75005, C75003[7][8]
On focus list of Wikimedia project
WikiProject Medicine[11]
P14914
D295195[13]
🏷️ Also known as
en syndactyly type 2 en synpolydactyly fr synpolydactylie ja 多合指症
🔖 Identifiers · 13
BabelNet ID
01450248n
Disease Ontology ID
DOID:0060242
DiseasesDB
33019
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
GARD rare disease ID
5087
KEGG ID
H00459
MeSH descriptor ID
C538153
Microsoft Academic ID (discontinued)
2781259359
Mondo ID
MONDO_0021651
OMIM ID
610k (186k–610k, n=3)
Orphanet ID
295195
UMLS CUI
C2699746
Show all 13 identifiers +1
WikiProjectMed ID
Synpolydactyly

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Summary

synpolydactyly is a rare disease[1]. synpolydactyly is a type of syndactyly[2], polydactyly[3], dysostosis of genetic origin with limb anomaly as a major feature[4], and developmental defect during embryogenesis[5].

References

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

Direct Wikidata claims

  1. [6] ↑ . wikidata.org.
  2. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [3] ↑ . wikidata.org.
  4. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [9] ↑ . The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly. wikidata.org.
  9. [10] ↑ . Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . 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). synpolydactyly. Retrieved November 6, 2026, from https://4ort.xyz/entity/synpolydactyly
MLA “synpolydactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/synpolydactyly.
BibTeX @misc{4ortxyz_synpolydactyly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{synpolydactyly}}, year = {2026}, url = {https://4ort.xyz/entity/synpolydactyly}, note = {Accessed: 2026-11-06}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): synpolydactyly — https://4ort.xyz/entity/synpolydactyly (retrieved 2026-11-06)

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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. 14d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Sitelink count → 1
    Wikipedia languages → ['en']
    Has phenotype → preaxial Hallucal polydactyly
    P14914 → D295195
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo ID → MONDO_0021651
    Orphanet ID → 295195
    BabelNet ID → 01450248n
    Imported from → —
    + 16 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"
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