inherited pseudoxanthoma elasticum

Human disease
MedicalCondition designated_intractable_rare_disease Q1052391
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inherited pseudoxanthoma elasticum

Summary

inherited pseudoxanthoma elasticum is a designated intractable/rare disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • inherited pseudoxanthoma elasticum's instance of is recorded as designated intractable/rare disease[3].
  • inherited pseudoxanthoma elasticum's instance of is recorded as developmental defect during embryogenesis[4].
  • inherited pseudoxanthoma elasticum's instance of is recorded as rare disease[5].
  • inherited pseudoxanthoma elasticum's instance of is recorded as class of disease[6].
  • inherited pseudoxanthoma elasticum is a type of autosomal recessive disease[7].
  • inherited pseudoxanthoma elasticum is a type of connective tissue disease[8].
  • inherited pseudoxanthoma elasticum is a type of genetic central nervous system and retinal vascular disease[9].
  • inherited pseudoxanthoma elasticum is a type of central nervous system and retinal vascular disease[10].
  • inherited pseudoxanthoma elasticum is a type of dermis elastic tissue disorder[11].
  • inherited pseudoxanthoma elasticum is a type of familial restrictive cardiomyopathy[12].
  • inherited pseudoxanthoma elasticum is a type of connective tissue disease with eye involvement[13].
  • inherited pseudoxanthoma elasticum is a type of malformation syndrome with skin/mucosae involvement[14].
  • inherited pseudoxanthoma elasticum is a type of rare developmental defect with connective tissue involvement[15].
  • inherited pseudoxanthoma elasticum is a type of inherited or acquired pseudoxanthoma elasticum[16].
  • inherited pseudoxanthoma elasticum is a type of genetic hypertension[17].
  • inherited pseudoxanthoma elasticum's Commons category is recorded as Pseudoxanthoma elasticum[18].
  • inherited pseudoxanthoma elasticum's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4579[19].
  • inherited pseudoxanthoma elasticum's ICD-9-CM is recorded as 757.39[20].
  • inherited pseudoxanthoma elasticum's NCI Thesaurus ID is recorded as C85036[21].
  • inherited pseudoxanthoma elasticum's health specialty is recorded as medical genetics[22].
  • inherited pseudoxanthoma elasticum's genetic association is recorded as ABCC6[23].
  • inherited pseudoxanthoma elasticum's genetic association is recorded as XYLT2[24].
  • inherited pseudoxanthoma elasticum's genetic association is recorded as XYLT1[25].
  • inherited pseudoxanthoma elasticum's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2738[26].
  • inherited pseudoxanthoma elasticum's exact match is recorded as http://identifiers.org/doid/DOID:2738[27].

Why It Matters

inherited pseudoxanthoma elasticum has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 18 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  18. [20] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] . Disease Ontology. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  22. [24] . Q905695. Retrieved . wikidata.org.
  23. [25] . Q905695. Retrieved . wikidata.org.
  24. [26] . Disease Ontology. Retrieved . wikidata.org.
  25. [27] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . 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). inherited pseudoxanthoma elasticum. Retrieved May 3, 2026, from https://4ort.xyz/entity/inherited-pseudoxanthoma-elasticum
MLA “inherited pseudoxanthoma elasticum.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/inherited-pseudoxanthoma-elasticum.
BibTeX @misc{4ortxyz_inherited-pseudoxanthoma-elasticum_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{inherited pseudoxanthoma elasticum}}, year = {2026}, url = {https://4ort.xyz/entity/inherited-pseudoxanthoma-elasticum}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): inherited pseudoxanthoma elasticum — https://4ort.xyz/entity/inherited-pseudoxanthoma-elasticum (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. 26d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of autosomal recessive disease, connective tissue disease, genetic central nervous system and retinal vascular disease +8
    Health specialty medical genetics
    Genetic association ABCC6, XYLT2, XYLT1
    Subclass of
    + 4 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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