ectrodactyly

deficiency or absence of one or more central digits of the hand or foot
MedicalCondition rare_disease Q650026
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ectrodactyly

Summary

ectrodactyly is a rare disease[1]. ectrodactyly draws 37 Wikipedia views per month (rare_disease category, ranking #69 of 627).[2]

Key Facts

  • ectrodactyly's instance of is recorded as rare disease[3].
  • ectrodactyly's instance of is recorded as class of disease[4].
  • ectrodactyly is a type of dysmelia[5].
  • ectrodactyly is a type of split hand-foot malformation[6].
  • ectrodactyly is a type of genetic disease[7].
  • ectrodactyly is a type of autosomal recessive disease[8].
  • ectrodactyly's Commons category is recorded as Ectrodactyly[9].
  • ectrodactyly's ICPC 2 ID is recorded as L82[10].
  • ectrodactyly's ICD-9-CM is recorded as 755.58[11].
  • ectrodactyly's NCI Thesaurus ID is recorded as C75000[12].
  • ectrodactyly's health specialty is recorded as medical genetics[13].
  • ectrodactyly's genetic association is recorded as WNT10B[14].
  • ectrodactyly's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090026[15].
  • ectrodactyly's exact match is recorded as http://identifiers.org/doid/DOID:0090026[16].
  • ectrodactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2440[17].
  • ectrodactyly's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].

Why It Matters

ectrodactyly draws 37 Wikipedia views per month (rare_disease category, ranking #69 of 627).[2] ectrodactyly has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[19] ectrodactyly is known by 18 alternative names across languages and contexts.[20]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation. wikidata.org.
  13. [15] ↑ . Disease Ontology. Retrieved . wikidata.org.
  14. [16] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [19] ↑ . Wikidata sitelinks. wikidata.org.
  3. [20] ↑ . Wikidata aliases. 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). ectrodactyly. Retrieved October 4, 2026, from https://4ort.xyz/entity/ectrodactyly
MLA “ectrodactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Oct. 2026, https://4ort.xyz/entity/ectrodactyly.
BibTeX @misc{4ortxyz_ectrodactyly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ectrodactyly}}, year = {2026}, url = {https://4ort.xyz/entity/ectrodactyly}, note = {Accessed: 2026-10-04}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ectrodactyly — https://4ort.xyz/entity/ectrodactyly (retrieved 2026-10-04)

Canonical URL: https://4ort.xyz/entity/ectrodactyly · 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. 3h ago · عُثمان · 2026-10-04 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'az', 'bg', 'commons', 'de', 'en', 'eo', 'es', 'fa', 'fi', 'fr', 'he', 'i
    Human phenotype ontology id → HP:0100257
    Claims rich → —
    "/* wbsetclaim-create:1||1 */ [[Property:P3841]]: HP:0100257, Matched to [[:toollabs:mix-n-match/#/entry/19251908|Ectrodactyly (#19251908)]] in [[:toollabs:mix-n-match/#/catalog/405|HPO]] #mix'n'match"
  2. 13w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Health specialty → medical genetics
    Genetic association → WNT10B
    Subclass of → —
    Instance of → rare disease, class of disease
    + 4 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.