Fabry disease

rare human genetic lysosomal storage disorder
MedicalCondition rare_disease Q615645
Fabry disease
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Summary

Fabry disease is a rare disease[1]. It ranks in the top 3% of rare_disease entities by monthly Wikipedia readership (381 views/month).[2]

Key Facts

  • Fabry disease's instance of is recorded as rare disease[3].
  • Fabry disease's instance of is recorded as class of disease[4].
  • Fabry disease's instance of is recorded as symptom or sign[5].
  • Johannes Fabry is named after Fabry disease[6].
  • Fabry disease is a type of sphingolipidosis[7].
  • Fabry disease is a type of developmental anomaly of metabolic origin[8].
  • Fabry disease is a type of genetic skin vascular disorder[9].
  • Fabry disease is a type of rare genetic epilepsy[10].
  • Fabry disease is a type of syndromic dyslipidemia[11].
  • Fabry disease is a type of vascular skin disease[12].
  • Fabry disease is a type of hypertrophic cardiomyopathy[13].
  • Fabry disease is a type of sphingolipidosis with epilepsy[14].
  • Fabry disease is a type of syndromic lymphedema[15].
  • Fabry disease is a type of nephropathy secondary to a storage or other metabolic disease[16].
  • Fabry disease is a type of cataract associated with a metabolic disease[17].
  • Fabry disease is a type of metabolic disease with corneal opacity[18].
  • Fabry disease is a type of lysosomal disease with restrictive cardiomyopathy[19].
  • Fabry disease is a type of lysosomal disease with hypertrophic cardiomyopathy[20].
  • Fabry disease is a type of rare hereditary metabolic disease with peripheral neuropathy[21].
  • Fabry disease is a type of syndrome associated with hypertrophic cardiomyopathy[22].
  • Fabry disease is a type of developmental defect during embryogenesis[23].
  • Fabry disease is a type of genetic disease[24].
  • Fabry disease's Commons category is recorded as Fabry disease[25].
  • Fabry disease's ICPC 2 ID is recorded as T99[26].
  • Fabry disease's symptoms and signs is recorded as pain[27].

Why It Matters

Fabry disease ranks in the top 3% of rare_disease entities by monthly Wikipedia readership (381 views/month).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 45 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . 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). Fabry disease. Retrieved October 14, 2026, from https://4ort.xyz/entity/fabry-disease
MLA “Fabry disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 14 Oct. 2026, https://4ort.xyz/entity/fabry-disease.
BibTeX @misc{4ortxyz_fabry-disease_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Fabry disease}}, year = {2026}, url = {https://4ort.xyz/entity/fabry-disease}, note = {Accessed: 2026-10-14}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Fabry disease — https://4ort.xyz/entity/fabry-disease (retrieved 2026-10-14)

Canonical URL: https://4ort.xyz/entity/fabry-disease · Last refreshed:

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. 18d ago · فيصل · 2026-09-26 view diff on Wikidata ↗
    Described by source → The Unified dictionary of genetics terms
    "/* wbsetclaim-create:2||1 */ Described by source: The Unified dictionary of genetics terms"
  2. 29d ago · Ksn.kenny · 2026-09-15 view diff on Wikidata ↗
    National library of spain spmabn id (bne v1.0) → XX5043143
    "/* wbsetclaim-create:2||1 */ National library of spain spmabn id (bne v1.0): XX5043143"
  3. 13w ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    P14541 → CCX1A
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
  4. 14w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Subclass of → sphingolipidosis, developmental anomaly of metabolic origin, genetic skin vascular disorder +15
    Instance of → rare disease, class of disease, symptom or sign
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
  5. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → sphingolipidosis, developmental anomaly of metabolic origin, genetic skin vascular disorder +15
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
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