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fundus dystrophy

human disease
Class type of: eye disease, retinal degeneration, genetic vitreous-retinal disease Q5811451

Facts

7 properties
Instance of
class of disease
Subclass of
eye disease, retinal degeneration, genetic vitreous-retinal disease
Genetic association
RLBP1, RDH5, LCA5, RPE65, OTX2, CLEC3B, HKDC1, ABCA4, ACO2, ADAM9, AHR, AIPL1, BBS1, BBS2, CACNA1F, CDH3, CLDN19, CNGA1, CNGA3, CRX, FBLN5, FBN2, GNAT2, IDH3A, IMPDH1, KIF11, LRAT, MAK, MERTK, OAT, PAX6, PDE6A, PDE6G, PROM1, RAB28, RBP4, OPN1LW, PRPH2, RHO, GRK1, ROM1, RP1, RPGR, RS1, SAG, TINF2, TREX1, USH2A, BEST1, ARL6, RPGRIP1, PRPF31, KIZ, RP1L1, ARHGEF18, ARL2BP, PRPF3, TUBGCP6, RCBTB1, RAX2, IMPG2, TTC8, SPATA7, TUBB4B, TOPORS, CERKL, CYP4V2, LRIT3, TLCD3B, FAM161A, CFAP418, MFSD8, CEP290, IFT140, SLC7A14, IFT172, SNRNP200, GPR179, PRCD, PCARE[9][10][11][12][13][14][15][16][17][18][19][20][21][22]
Health specialty
ophthalmology[8]
ICD-9-CM
362.75, 362.72[5][6]
NCI Thesaurus ID
C35625[7]
On focus list of Wikimedia project
WikiProject Medicine
🏷️ Also known as
en Retinal Dystrophy en fundus dystrophies en fundus dystrophy en retinal dystrophies de Netzhautdystrophie es Distrofias de la retina fr dystrophie de la rétine fr dystrophie du fond d'oeil
🔖 Identifiers · 10
Disease Ontology ID
DOID:8501
DiseasesDB
9580
Exact match
purl.obolibrary.org, identifiers.org, purl.obolibrary.org, www.orpha.net
Human Phenotype Ontology ID
HP:0000556
MeSH descriptor ID
D058499
MeSH tree code
C11.768.585.658
Mondo ID
MONDO_0019118
Orphanet ID
71862
Raras disease ID
D71862
UMLS CUI
C0854723

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Summary

fundus dystrophy is a class of disease[1]. It is a type of eye disease[2], retinal degeneration[3], and genetic vitreous-retinal disease[4].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  9. [10] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  10. [11] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  11. [12] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  12. [13] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). fundus dystrophy. Retrieved November 11, 2026, from https://4ort.xyz/entity/fundus-dystrophy
MLA “fundus dystrophy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 11 Nov. 2026, https://4ort.xyz/entity/fundus-dystrophy.
BibTeX @misc{4ortxyz_fundus-dystrophy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fundus dystrophy}}, year = {2026}, url = {https://4ort.xyz/entity/fundus-dystrophy}, note = {Accessed: 2026-11-11}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): fundus dystrophy — https://4ort.xyz/entity/fundus-dystrophy (retrieved 2026-11-11)

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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. 19d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Genetic association → RLBP1, RDH5, LCA5 +1
    Raras disease ID → D71862
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    NCI Thesaurus ID → C35625
    On focus list of Wikimedia project → WikiProject Medicine
    Health specialty → ophthalmology
    ICD-9-CM → 362.75, 362.72
    + 13 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39953: deprecate redundant disease superclasses (2)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.