vitelliform macular dystrophy

macular degeneration that can cause progressive vision loss, it is characterized by the disruption of cells in a small area near the center of the retina, the macula
MedicalCondition rare_disease Q830265
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vitelliform macular dystrophy

Summary

vitelliform macular dystrophy is a rare disease[1]. It draws 23 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2]

Key Facts

  • vitelliform macular dystrophy's instance of is recorded as rare disease[3].
  • vitelliform macular dystrophy's instance of is recorded as class of disease[4].
  • vitelliform macular dystrophy's subclass of is recorded as macular degeneration[5].
  • vitelliform macular dystrophy's MeSH descriptor ID is recorded as D057826[6].
  • vitelliform macular dystrophy's OMIM ID is recorded as 616152[7].
  • vitelliform macular dystrophy's OMIM ID is recorded as 153840[8].
  • vitelliform macular dystrophy's OMIM ID is recorded as 608161[9].
  • vitelliform macular dystrophy's OMIM ID is recorded as 153700[10].
  • vitelliform macular dystrophy's OMIM ID is recorded as 616151[11].
  • vitelliform macular dystrophy's DiseasesDB is recorded as 34190[12].
  • vitelliform macular dystrophy's Freebase ID is recorded as /m/0cw6_p[13].
  • vitelliform macular dystrophy's KEGG ID is recorded as H00814[14].
  • vitelliform macular dystrophy's MeSH tree code is recorded as C11.768.585.439.433[15].
  • vitelliform macular dystrophy's MeSH tree code is recorded as C16.320.290.763[16].
  • vitelliform macular dystrophy's eMedicine ID is recorded as 1227128[17].
  • vitelliform macular dystrophy's Disease Ontology ID is recorded as DOID:0050661[18].
  • vitelliform macular dystrophy's Orphanet ID is recorded as 1243[19].
  • vitelliform macular dystrophy's Orphanet ID is recorded as 99000[20].
  • vitelliform macular dystrophy's NCI Thesaurus ID is recorded as C118788[21].
  • vitelliform macular dystrophy's health specialty is recorded as ophthalmology[22].
  • vitelliform macular dystrophy's health specialty is recorded as medical genetics[23].
  • vitelliform macular dystrophy's genetic association is recorded as IMPG2[24].
  • vitelliform macular dystrophy's genetic association is recorded as IMPG1[25].
  • vitelliform macular dystrophy's genetic association is recorded as PRPH2[26].
  • vitelliform macular dystrophy's genetic association is recorded as BEST1[27].

Why It Matters

vitelliform macular dystrophy draws 23 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] It is known by 9 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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . Disease Ontology. Retrieved . wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . Frequency and Clinical Pattern of Vitelliform Macular Dystrophy Caused by Mutations of Interphotoreceptor Matrix IMPG1 and IMPG2 Genes. wikidata.org.
  23. [25] . Mutations in IMPG1 cause vitelliform macular dystrophies.. wikidata.org.
  24. [26] . Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. wikidata.org.
  25. [27] . Identification of the gene responsible for Best macular dystrophy. 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.

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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). vitelliform macular dystrophy. Retrieved May 3, 2026, from https://4ort.xyz/entity/vitelliform-macular-dystrophy
MLA “vitelliform macular dystrophy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vitelliform-macular-dystrophy.
BibTeX @misc{4ortxyz_vitelliform-macular-dystrophy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vitelliform macular dystrophy}}, year = {2026}, url = {https://4ort.xyz/entity/vitelliform-macular-dystrophy}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vitelliform macular dystrophy — https://4ort.xyz/entity/vitelliform-macular-dystrophy (retrieved 2026-05-03)

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