Stargardt disease

age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness
MedicalCondition rare_disease Q1317319
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Stargardt disease

Summary

Stargardt disease is a rare disease[1]. It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • Stargardt disease's instance of is recorded as rare disease[3].
  • Stargardt disease's instance of is recorded as class of disease[4].
  • Stargardt disease is a type of age related macular degeneration[5].
  • Stargardt disease is a type of disease[6].
  • Stargardt disease's Commons category is recorded as Stargardt disease[7].
  • Stargardt disease's health specialty is recorded as ophthalmology[8].
  • Stargardt disease's genetic association is recorded as ABCA4[9].
  • Stargardt disease's genetic association is recorded as CNGB3[10].
  • Stargardt disease's genetic association is recorded as PROM1[11].
  • Stargardt disease's genetic association is recorded as ELOVL4[12].
  • Stargardt disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050817[13].
  • Stargardt disease's exact match is recorded as http://identifiers.org/doid/DOID:0050817[14].
  • Stargardt disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_364055[15].
  • Stargardt disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_827[16].
  • Stargardt disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].

Why It Matters

Stargardt disease has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2] It is known by 16 alternative names across languages and contexts.[18]

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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [10] . Q905695. Retrieved . wikidata.org.
  9. [11] . Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice. wikidata.org.
  10. [12] . A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. wikidata.org.
  11. [13] . Disease Ontology. Retrieved . wikidata.org.
  12. [14] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [18] . 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). Stargardt disease. Retrieved May 3, 2026, from https://4ort.xyz/entity/stargardt-disease
MLA “Stargardt disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/stargardt-disease.
BibTeX @misc{4ortxyz_stargardt-disease_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Stargardt disease}}, year = {2026}, url = {https://4ort.xyz/entity/stargardt-disease}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Stargardt disease — https://4ort.xyz/entity/stargardt-disease (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/stargardt-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. 8d ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    P14541 35CsEl
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
  2. 16d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of age related macular degeneration, disease
    Health specialty ophthalmology
    Genetic association ABCA4, CNGB3, PROM1 +1
    Subclass of
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
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