Czech dysplasia, metatarsal type

Czech dysplasia, metatarsal type is a form of skeletal dysplasia characterised by severe arthropathy beginning in childhood and hypoplasia/dysplasia of the third, fourth and/or fifth toes
MedicalCondition developmental_defect_during_embryogenesis Q55783645
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Czech dysplasia, metatarsal type

Summary

Czech dysplasia, metatarsal type is a developmental defect during embryogenesis[1].

Key Facts

  • Czech dysplasia, metatarsal type's instance of is recorded as developmental defect during embryogenesis[2].
  • Czech dysplasia, metatarsal type's instance of is recorded as rare disease[3].
  • Czech dysplasia, metatarsal type's instance of is recorded as class of disease[4].
  • Czech dysplasia, metatarsal type is a type of type 2 collagen-related bone disorder[5].
  • Czech dysplasia, metatarsal type is a type of spondyloepimetaphyseal dysplasia[6].
  • Czech dysplasia, metatarsal type's genetic association is recorded as COL2A1[7].
  • Czech dysplasia, metatarsal type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_137678[8].

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APA 4ort.xyz Knowledge Graph. (2026). Czech dysplasia, metatarsal type. Retrieved May 3, 2026, from https://4ort.xyz/entity/czech-dysplasia-metatarsal-type
MLA “Czech dysplasia, metatarsal type.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/czech-dysplasia-metatarsal-type.
BibTeX @misc{4ortxyz_czech-dysplasia-metatarsal-type_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Czech dysplasia, metatarsal type}}, year = {2026}, url = {https://4ort.xyz/entity/czech-dysplasia-metatarsal-type}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Czech dysplasia, metatarsal type — https://4ort.xyz/entity/czech-dysplasia-metatarsal-type (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. 3h ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0012206
    Genetic association COL2A1
    Gard rare disease id 10220
    Orphanet id 137678
    + 11 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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