Waardenburg syndrome type 2D

human disease
MedicalCondition rare_disease Q32145160
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Waardenburg syndrome type 2D

Summary

Waardenburg syndrome type 2D is a rare disease[1].

Key Facts

  • Waardenburg syndrome type 2D's instance of is recorded as rare disease[2].
  • Waardenburg syndrome type 2D's instance of is recorded as class of disease[3].
  • Waardenburg syndrome type 2D is a type of Waardenburg's syndrome[4].
  • Waardenburg syndrome type 2D is a type of disease[5].
  • Waardenburg syndrome type 2D's genetic association is recorded as SNAI2[6].
  • Waardenburg syndrome type 2D's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110952[7].
  • Waardenburg syndrome type 2D's exact match is recorded as http://identifiers.org/doid/DOID:0110952[8].
  • Waardenburg syndrome type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3440[9].
  • Waardenburg syndrome type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_895[10].
  • Waardenburg syndrome type 2D's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].

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APA 4ort.xyz Knowledge Graph. (2026). Waardenburg syndrome type 2D. Retrieved May 3, 2026, from https://4ort.xyz/entity/waardenburg-syndrome-type-2d
MLA “Waardenburg syndrome type 2D.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/waardenburg-syndrome-type-2d.
BibTeX @misc{4ortxyz_waardenburg-syndrome-type-2d_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Waardenburg syndrome type 2D}}, year = {2026}, url = {https://4ort.xyz/entity/waardenburg-syndrome-type-2d}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Waardenburg syndrome type 2D — https://4ort.xyz/entity/waardenburg-syndrome-type-2d (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. 1d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0012144
    Genetic association SNAI2
    Instance of rare disease, class of disease
    Imported from
    + 9 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
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