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syndactyly

synostosis that results in the fusion of two or more digits
Class type of: synostosis, congenital limb deformity, chromosomal duplication syndrome Q1360044
syndactyly
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Facts

9 properties
Instance of
rare disease, class of disease[2]
Subclass of
synostosis, congenital limb deformity, chromosomal duplication syndrome[3][4][5]
Described by source
Armenian Soviet Encyclopedia, vol. 7[7]
Genetic association
HOXD13, LMBR1, GJA1[11][12][13]
Health specialty
medical genetics[10]
ICD-9-CM
755.1[8]
ICPC 2 ID
L82[6]
NCI Thesaurus ID
C87125[9]
On focus list of Wikimedia project
WikiProject Medicine[14]
🏷️ Also known as
en syndactyly en Syndactyly, mitten type en Unilateral syndactyly of digits 2-5 en webbing of digits en chromosome 2q35 duplication syndrome en Mitten hand en symphalangism en symphalangy en symphalangy (disorder) ar التصاق الأصابع ar تكفف الأصابع ar ارتفاق الأصابع de Syndaktylie es sindactilia es sinfalangia es sinfalangismo fa سینداکتیلی fi Yhdyssormisuus fi Räpyläjalkaisuus fi Räpyläkätisyys
🔖 Identifiers · 29
OpenAlex ID
C2777202849
BabelNet ID
00075711n
Disease Ontology ID
DOID:11193
DiseasesDB
29330
EMedicine ID
1244420
Elhuyar ZTH ID
030705
Encyclopædia Britannica Online ID
science/syndactyly
Exact match
purl.obolibrary.org, identifiers.org, purl.obolibrary.org, www.orpha.net, www.orpha.net, www.orpha.net, www.orpha.net, www.orpha.net, www.orpha.net
Freebase ID
/m/03gq490
GARD rare disease ID
13181
Great Russian Encyclopedia portal ID
sindaktiliia-08925e
Human Phenotype Ontology ID
HP:0001159
Show all 29 identifiers +17
ICD-10-CM
Q70.9, Bern, Q70.1
ICD-11 ID (Foundation)
1736296640
ICD-11 ID (MMS)
LB79
JSTOR topic ID (archived)
syndactyly
KEGG ID
H01095
MeSH descriptor ID
D013576
MeSH tree code
C05.116.099.370.894.819, C05.660.585.800, C05.660.906.819, C16.131.621.585.800, C16.131.621.906.819
MedlinePlus ID
003289
Microsoft Academic ID (discontinued)
2777202849
Mondo ID
MONDO_0017460
OMIM ID
186k (186k–186k, n=4)
OmegaWiki Defined Meaning
1351872
Orphanet ID
295k (90k–295k, n=6)
PatientsLikeMe condition ID
syndactyly
Store medisinske leksikon ID
syndaktyli
UMLS CUI
C0039075, C1861348, C1861366, C4706525, C5681365
WordNet 3.1 Synset ID
14495510-n

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

🔗 Connections
Genetic association 3
GJA1, HOXD13, LMBR1
← Medical condition 3
Ashton Kutcher, Dan Aykroyd, Almudena Cid
Subclass of 2
disease, synostosis
Subtypes 2
acrocephalosyndactylia, webbed toes
Health specialty 1
medical genetics
ICD-10-CM 1
Bern
Instance of 1
rare disease
On focus list of Wikimedia project 1
WikiProject Medicine
← Genetic association 1
HOXD13
← Has phenotype 1
acrocephalosyndactylia
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Summary

syndactyly is a rare disease[1].

Related Entities

Ashton Kutcher Bern Dan Aykroyd disease

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  11. [12] ↑ . Triphalangeal thumb-polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer. wikidata.org.
  12. [13] ↑ . Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. wikidata.org.
  13. [14] ↑ . 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). syndactyly. Retrieved November 6, 2026, from https://4ort.xyz/entity/syndactyly
MLA “syndactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/syndactyly.
BibTeX @misc{4ortxyz_syndactyly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{syndactyly}}, year = {2026}, url = {https://4ort.xyz/entity/syndactyly}, note = {Accessed: 2026-11-06}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): syndactyly — https://4ort.xyz/entity/syndactyly (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. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → synostosis, congenital limb deformity, chromosomal duplication syndrome
    On focus list of Wikimedia project → WikiProject Medicine
    Health specialty → medical genetics
    Genetic association → HOXD13, LMBR1, GJA1
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.