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spondyloepimetaphyseal dysplasia, matrilin-3 type

MedicalCondition developmental_defect_during_embryogenesis Q55783602
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spondyloepimetaphyseal dysplasia, matrilin-3 type

Summary

spondyloepimetaphyseal dysplasia, matrilin-3 type is a developmental defect during embryogenesis[1].

Key Facts

  • spondyloepimetaphyseal dysplasia, matrilin-3 type's instance of is recorded as developmental defect during embryogenesis[2].
  • spondyloepimetaphyseal dysplasia, matrilin-3 type's instance of is recorded as rare disease[3].
  • spondyloepimetaphyseal dysplasia, matrilin-3 type's instance of is recorded as class of disease[4].
  • spondyloepimetaphyseal dysplasia, matrilin-3 type is a type of disease[5].
  • spondyloepimetaphyseal dysplasia, matrilin-3 type's genetic association is recorded as MATN3[6].
  • spondyloepimetaphyseal dysplasia, matrilin-3 type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_156728[7].

References

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

Direct Wikidata claims

  1. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Q905695. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

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APA 4ort.xyz Knowledge Graph. (2026). spondyloepimetaphyseal dysplasia, matrilin-3 type. Retrieved May 3, 2026, from https://4ort.xyz/entity/spondyloepimetaphyseal-dysplasia-matrilin-3-type
MLA “spondyloepimetaphyseal dysplasia, matrilin-3 type.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/spondyloepimetaphyseal-dysplasia-matrilin-3-type.
BibTeX @misc{4ortxyz_spondyloepimetaphyseal-dysplasia-matrilin-3-type_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spondyloepimetaphyseal dysplasia, matrilin-3 type}}, year = {2026}, url = {https://4ort.xyz/entity/spondyloepimetaphyseal-dysplasia-matrilin-3-type}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): spondyloepimetaphyseal dysplasia, matrilin-3 type — https://4ort.xyz/entity/spondyloepimetaphyseal-dysplasia-matrilin-3-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. 8d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Instance of → developmental defect during embryogenesis, rare disease, class of disease
    Subclass of → disease
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
  2. 8d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0012108
    Genetic association → MATN3
    Kegg id → H00767
    Orphanet id → 156728
    + 9 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"
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