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autosomal dominant vitreoretinochoroidopathy

MedicalCondition rare_disease Q55345683
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autosomal dominant vitreoretinochoroidopathy

Summary

autosomal dominant vitreoretinochoroidopathy is a rare disease[1].

Key Facts

  • autosomal dominant vitreoretinochoroidopathy's instance of is recorded as rare disease[2].
  • autosomal dominant vitreoretinochoroidopathy's instance of is recorded as class of disease[3].
  • autosomal dominant vitreoretinochoroidopathy's subclass of is recorded as vitreoretinal degeneration[4].
  • autosomal dominant vitreoretinochoroidopathy's subclass of is recorded as hereditary retinal dystrophy[5].
  • autosomal dominant vitreoretinochoroidopathy's subclass of is recorded as autosomal dominant disease[6].
  • autosomal dominant vitreoretinochoroidopathy's MeSH descriptor ID is recorded as C536352[7].
  • autosomal dominant vitreoretinochoroidopathy's OMIM ID is recorded as 193220[8].
  • autosomal dominant vitreoretinochoroidopathy's KEGG ID is recorded as H02078[9].
  • autosomal dominant vitreoretinochoroidopathy's Disease Ontology ID is recorded as DOID:0111569[10].
  • autosomal dominant vitreoretinochoroidopathy's Orphanet ID is recorded as 3086[11].
  • autosomal dominant vitreoretinochoroidopathy's genetic association is recorded as BEST1[12].
  • autosomal dominant vitreoretinochoroidopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_263347[13].
  • autosomal dominant vitreoretinochoroidopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3086[14].
  • autosomal dominant vitreoretinochoroidopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111569[15].
  • autosomal dominant vitreoretinochoroidopathy's exact match is recorded as http://identifiers.org/doid/DOID:0111569[16].
  • autosomal dominant vitreoretinochoroidopathy's UMLS CUI is recorded as C3888099[17].
  • autosomal dominant vitreoretinochoroidopathy's UMLS CUI is recorded as C2674009[18].
  • autosomal dominant vitreoretinochoroidopathy's UMLS CUI is recorded as C1860406[19].
  • autosomal dominant vitreoretinochoroidopathy's ICD-10-CM is recorded as H35.5[20].
  • autosomal dominant vitreoretinochoroidopathy's GARD rare disease ID is recorded as 5507[21].
  • autosomal dominant vitreoretinochoroidopathy's Mondo ID is recorded as MONDO_0008662[22].
  • autosomal dominant vitreoretinochoroidopathy's ICD-11 ID is recorded as 96951767[23].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [12] ↑ . Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC).. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [16] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  16. [17] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [18] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [19] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [20] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). autosomal dominant vitreoretinochoroidopathy. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-vitreoretinochoroidopathy
MLA “autosomal dominant vitreoretinochoroidopathy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-vitreoretinochoroidopathy.
BibTeX @misc{4ortxyz_autosomal-dominant-vitreoretinochoroidopathy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant vitreoretinochoroidopathy}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-vitreoretinochoroidopathy}, note = {Accessed: 2026-05-03}}
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