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 ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (328 views/month).[2]

Key Facts

  • Fabry disease's image is recorded as PBB Protein GLA image.jpg[3].
  • Fabry disease's instance of is recorded as developmental defect during embryogenesis[4].
  • Fabry disease's instance of is recorded as rare disease[5].
  • Fabry disease's instance of is recorded as genetic disease[6].
  • Fabry disease's instance of is recorded as class of disease[7].
  • Fabry disease's instance of is recorded as symptom or sign[8].
  • Johannes Fabry is named after Fabry disease[9].
  • Fabry disease's GND ID is recorded as 4153455-4[10].
  • Fabry disease's subclass of is recorded as sphingolipidosis[11].
  • Fabry disease's subclass of is recorded as developmental anomaly of metabolic origin[12].
  • Fabry disease's subclass of is recorded as genetic skin vascular disorder[13].
  • Fabry disease's subclass of is recorded as rare genetic epilepsy[14].
  • Fabry disease's subclass of is recorded as syndromic dyslipidemia[15].
  • Fabry disease's subclass of is recorded as vascular skin disease[16].
  • Fabry disease's subclass of is recorded as hypertrophic cardiomyopathy[17].
  • Fabry disease's subclass of is recorded as sphingolipidosis with epilepsy[18].
  • Fabry disease's subclass of is recorded as syndromic lymphedema[19].
  • Fabry disease's subclass of is recorded as nephropathy secondary to a storage or other metabolic disease[20].
  • Fabry disease's subclass of is recorded as cataract associated with a metabolic disease[21].
  • Fabry disease's subclass of is recorded as metabolic disease with corneal opacity[22].
  • Fabry disease's subclass of is recorded as lysosomal disease with restrictive cardiomyopathy[23].
  • Fabry disease's subclass of is recorded as lysosomal disease with hypertrophic cardiomyopathy[24].
  • Fabry disease's subclass of is recorded as rare hereditary metabolic disease with peripheral neuropathy[25].
  • Fabry disease's subclass of is recorded as syndrome associated with hypertrophic cardiomyopathy[26].
  • Fabry disease's subclass of is recorded as disease[27].

Why It Matters

Fabry disease ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (328 views/month).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 26 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  24. [26] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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 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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