Ehlers-Danlos syndrome, periodontitis type

Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility
MedicalCondition developmental_defect_during_embryogenesis Q55780543
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Ehlers-Danlos syndrome, periodontitis type

Summary

Ehlers-Danlos syndrome, periodontitis type is a developmental defect during embryogenesis[1].

Key Facts

  • Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as developmental defect during embryogenesis[2].
  • Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as rare disease[3].
  • Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as class of disease[4].
  • Ehlers-Danlos syndrome, periodontitis type's subclass of is recorded as rare disease with odontological manifestation[5].
  • Ehlers-Danlos syndrome, periodontitis type's subclass of is recorded as Ehlers-Danlos syndrome[6].
  • Ehlers-Danlos syndrome, periodontitis type's MeSH descriptor ID is recorded as C562626[7].
  • Ehlers-Danlos syndrome, periodontitis type's OMIM ID is recorded as 130080[8].
  • Ehlers-Danlos syndrome, periodontitis type's KEGG ID is recorded as H02240[9].
  • Ehlers-Danlos syndrome, periodontitis type's Orphanet ID is recorded as 75392[10].
  • Ehlers-Danlos syndrome, periodontitis type's genetic association is recorded as C1R[11].
  • Ehlers-Danlos syndrome, periodontitis type's genetic association is recorded as C1S[12].
  • Ehlers-Danlos syndrome, periodontitis type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75392[13].
  • Ehlers-Danlos syndrome, periodontitis type's UMLS CUI is recorded as C0268347[14].
  • Ehlers-Danlos syndrome, periodontitis type's ICD-10-CM is recorded as Q79.6[15].
  • Ehlers-Danlos syndrome, periodontitis type's Mondo ID is recorded as MONDO_0007527[16].
  • Ehlers-Danlos syndrome, periodontitis type's ICD-11 ID is recorded as 893527307[17].

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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [11] . Q905695. Retrieved . wikidata.org.
  11. [12] . Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [15] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_ehlers-danlos-syndrome-periodontitis-type_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Ehlers-Danlos syndrome, periodontitis type}}, year = {2026}, url = {https://4ort.xyz/entity/ehlers-danlos-syndrome-periodontitis-type}, note = {Accessed: 2026-05-03}}
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