synpolydactyly

syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene
MedicalCondition developmental_defect_during_embryogenesis Q7662637
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synpolydactyly

Summary

synpolydactyly is a developmental defect during embryogenesis[1]. synpolydactyly draws 12 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]

Key Facts

  • synpolydactyly's instance of is recorded as developmental defect during embryogenesis[3].
  • synpolydactyly's instance of is recorded as rare disease[4].
  • synpolydactyly's instance of is recorded as class of disease[5].
  • synpolydactyly's subclass of is recorded as syndactyly[6].
  • synpolydactyly's subclass of is recorded as polydactyly[7].
  • synpolydactyly's subclass of is recorded as dysostosis of genetic origin with limb anomaly as a major feature[8].
  • synpolydactyly's MeSH descriptor ID is recorded as C538153[9].
  • synpolydactyly's OMIM ID is recorded as 186000[10].
  • synpolydactyly's OMIM ID is recorded as 608180[11].
  • synpolydactyly's OMIM ID is recorded as 610234[12].
  • synpolydactyly's DiseasesDB is recorded as 33019[13].
  • synpolydactyly's KEGG ID is recorded as H00459[14].
  • synpolydactyly's Disease Ontology ID is recorded as DOID:0060242[15].
  • synpolydactyly's Orphanet ID is recorded as 295195[16].
  • synpolydactyly's NCI Thesaurus ID is recorded as C75005[17].
  • synpolydactyly's NCI Thesaurus ID is recorded as C75003[18].
  • synpolydactyly's genetic association is recorded as FBLN1[19].
  • synpolydactyly's genetic association is recorded as HOXD13[20].
  • synpolydactyly's BabelNet ID is recorded as 01450248n[21].
  • synpolydactyly's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060242[22].
  • synpolydactyly's exact match is recorded as http://identifiers.org/doid/DOID:0060242[23].
  • synpolydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_295195[24].
  • synpolydactyly's UMLS CUI is recorded as C2699746[25].
  • synpolydactyly's GARD rare disease ID is recorded as 5087[26].
  • synpolydactyly's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].

Why It Matters

synpolydactyly draws 12 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly. wikidata.org.
  18. [20] . Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. wikidata.org.
  19. [21] . BabelNet. wikidata.org.
  20. [22] . Disease Ontology. Retrieved . wikidata.org.
  21. [23] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . Disease Ontology. Retrieved . wikidata.org.
  24. [26] . Disease Ontology. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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 May 3, 2026, from https://4ort.xyz/entity/synpolydactyly
MLA “synpolydactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 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: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): synpolydactyly — https://4ort.xyz/entity/synpolydactyly (retrieved 2026-05-03)

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