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retinal degeneration associated with rhodopsin mutations

retinitis pigmentosa that has material basis in mutation in the RHO gene on chromosome 3q22
MedicalCondition rare_disease Q7316761
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Summary

retinal degeneration associated with rhodopsin mutations is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: retinal degeneration[4], retinitis pigmentosa[5], genetic disease[6], autosomal recessive disease[7], autosomal dominant disease[8]
  • Genetic association: RHO[9]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0110372[10], http://identifiers.org/doid/DOID:0110372[11]
  • On focus list of Wikimedia project: WikiProject Medicine[12]

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). retinal degeneration associated with rhodopsin mutations. Retrieved October 17, 2026, from https://4ort.xyz/entity/retinal-degeneration-associated-with-rhodopsin-mutations
MLA “retinal degeneration associated with rhodopsin mutations.” 4ort.xyz Knowledge Graph, 4ort.xyz, 17 Oct. 2026, https://4ort.xyz/entity/retinal-degeneration-associated-with-rhodopsin-mutations.
BibTeX @misc{4ortxyz_retinal-degeneration-associated-with-rhodopsin-mutations_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{retinal degeneration associated with rhodopsin mutations}}, year = {2026}, url = {https://4ort.xyz/entity/retinal-degeneration-associated-with-rhodopsin-mutations}, note = {Accessed: 2026-10-17}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): retinal degeneration associated with rhodopsin mutations — https://4ort.xyz/entity/retinal-degeneration-associated-with-rhodopsin-mutations (retrieved 2026-10-17)

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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. 15w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo id → MONDO_0013395
    Imported from → —
    Umls cui → C3151001
    Disease ontology id → DOID:0110372
    + 13 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
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