cone dystrophy

inherited ocular disorder characterized by the loss of cone cells
MedicalCondition rare_disease Q147270
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cone dystrophy

Summary

cone dystrophy is a rare disease[1]. It draws 42 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2]

Key Facts

  • cone dystrophy's image is recorded as Fundus of a patient with cone rod dystrophy.png[3].
  • cone dystrophy's instance of is recorded as rare disease[4].
  • cone dystrophy's instance of is recorded as class of disease[5].
  • cone dystrophy's subclass of is recorded as retinal disease[6].
  • cone dystrophy's Commons category is recorded as Cone dystrophy[7].
  • cone dystrophy's MeSH descriptor ID is recorded as D000077765[8].
  • cone dystrophy's OMIM ID is recorded as 610024[9].
  • cone dystrophy's OMIM ID is recorded as 610356[10].
  • cone dystrophy's OMIM ID is recorded as 610478[11].
  • cone dystrophy's OMIM ID is recorded as 613093[12].
  • cone dystrophy's OMIM ID is recorded as 180020[13].
  • cone dystrophy's ICD-10 ID is recorded as H35.5[14].
  • cone dystrophy's MeSH tree code is recorded as C11.270.151[15].
  • cone dystrophy's MeSH tree code is recorded as C11.768.216[16].
  • cone dystrophy's Disease Ontology ID is recorded as DOID:0050795[17].
  • cone dystrophy's health specialty is recorded as ophthalmology[18].
  • cone dystrophy's genetic association is recorded as PDE6H[19].
  • cone dystrophy's genetic association is recorded as PDE6C[20].
  • cone dystrophy's genetic association is recorded as KCNV2[21].
  • cone dystrophy's genetic association is recorded as CACNA2D4[22].
  • cone dystrophy's BabelNet ID is recorded as 01749600n[23].
  • cone dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050795[24].
  • cone dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0050795[25].
  • cone dystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1871[26].
  • cone dystrophy's UMLS CUI is recorded as C1867326[27].

Why It Matters

cone dystrophy draws 42 Wikipedia views per month (rare_disease category, ranking #208 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 7 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] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . 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] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . Disease Ontology. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy. wikidata.org.
  18. [20] . Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.. wikidata.org.
  19. [21] . Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans. wikidata.org.
  20. [22] . Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy. wikidata.org.
  21. [23] . BabelNet. wikidata.org.
  22. [24] . Disease Ontology. Retrieved . wikidata.org.
  23. [25] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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). cone dystrophy. Retrieved May 3, 2026, from https://4ort.xyz/entity/cone-dystrophy
MLA “cone dystrophy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cone-dystrophy.
BibTeX @misc{4ortxyz_cone-dystrophy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cone dystrophy}}, year = {2026}, url = {https://4ort.xyz/entity/cone-dystrophy}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cone dystrophy — https://4ort.xyz/entity/cone-dystrophy (retrieved 2026-05-03)

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