Fabry disease

rare human genetic lysosomal storage disorder
MedicalCondition developmental_defect_during_embryogenesis Q615645
Fabry disease
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Fabry disease

Summary

Fabry disease is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2]

Key Facts

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

Why It Matters

Fabry disease has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2] It is known by 26 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [20] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  22. [24] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] . 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). Fabry disease. Retrieved May 3, 2026, from https://4ort.xyz/entity/fabry-disease
MLA “Fabry disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 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: 2026-05-03}}
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 2026-05-03)

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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. 4d 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"
  2. 9d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Subclass of sphingolipidosis, developmental anomaly of metabolic origin, genetic skin vascular disorder +14
    Instance of developmental defect during embryogenesis, rare disease, genetic disease +2
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
  3. 11d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of sphingolipidosis, developmental anomaly of metabolic origin, genetic skin vascular disorder +14
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
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