familial digital arthropathy-brachydactyly

MedicalCondition developmental_defect_during_embryogenesis Q55783477
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familial digital arthropathy-brachydactyly

Summary

familial digital arthropathy-brachydactyly is a developmental defect during embryogenesis[1].

Key Facts

  • familial digital arthropathy-brachydactyly's instance of is recorded as developmental defect during embryogenesis[2].
  • familial digital arthropathy-brachydactyly's instance of is recorded as rare disease[3].
  • familial digital arthropathy-brachydactyly's instance of is recorded as class of disease[4].
  • familial digital arthropathy-brachydactyly is a type of syndrome with brachydactyly[5].
  • familial digital arthropathy-brachydactyly is a type of TRPV4-related bone disorder[6].
  • familial digital arthropathy-brachydactyly's NCI Thesaurus ID is recorded as C175208[7].
  • familial digital arthropathy-brachydactyly's genetic association is recorded as TRPV4[8].
  • familial digital arthropathy-brachydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85169[9].

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APA 4ort.xyz Knowledge Graph. (2026). familial digital arthropathy-brachydactyly. Retrieved May 3, 2026, from https://4ort.xyz/entity/familial-digital-arthropathy-brachydactyly
MLA “familial digital arthropathy-brachydactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/familial-digital-arthropathy-brachydactyly.
BibTeX @misc{4ortxyz_familial-digital-arthropathy-brachydactyly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{familial digital arthropathy-brachydactyly}}, year = {2026}, url = {https://4ort.xyz/entity/familial-digital-arthropathy-brachydactyly}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): familial digital arthropathy-brachydactyly — https://4ort.xyz/entity/familial-digital-arthropathy-brachydactyly (retrieved 2026-05-03)

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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. 4d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0011732
    Genetic association TRPV4
    Kegg id H02062
    Orphanet id 85169
    + 10 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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