cataract 25

cataract that has material basis in variation in the region 15q21-q22
MedicalCondition developmental_defect_during_embryogenesis Q27674894
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cataract 25

Summary

cataract 25 is a developmental defect during embryogenesis[1].

Key Facts

  • cataract 25's instance of is recorded as developmental defect during embryogenesis[2].
  • cataract 25's instance of is recorded as class of disease[3].
  • cataract 25 is a type of cataract[4].
  • cataract 25's health specialty is recorded as medical genetics[5].
  • cataract 25's genetic association is recorded as CRYBA1[6].
  • cataract 25's genetic association is recorded as MIP[7].
  • cataract 25's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110254[8].
  • cataract 25's exact match is recorded as http://identifiers.org/doid/DOID:0110254[9].
  • cataract 25's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].

📑 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). cataract 25. Retrieved May 3, 2026, from https://4ort.xyz/entity/cataract-25
MLA “cataract 25.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cataract-25.
BibTeX @misc{4ortxyz_cataract-25_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cataract 25}}, year = {2026}, url = {https://4ort.xyz/entity/cataract-25}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cataract 25 — https://4ort.xyz/entity/cataract-25 (retrieved 2026-05-03)

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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. 18d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0020372
    Genetic association CRYBA1, MIP
    Orphanet id 98985
    Instance of developmental defect during embryogenesis, class of disease
    + 10 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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