hypotrichosis 3

hypotrichosis that has material basis in a autosomal dominant mutation of KRT74 on chromosome 12q13.13
MedicalCondition rare_disease Q32140250
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hypotrichosis 3

Summary

hypotrichosis 3 is a rare disease[1].

Key Facts

  • hypotrichosis 3's instance of is recorded as rare disease[2].
  • hypotrichosis 3's instance of is recorded as class of disease[3].
  • hypotrichosis 3 is a type of hypotrichosis[4].
  • hypotrichosis 3 is a type of genetic disease[5].
  • hypotrichosis 3 is a type of autosomal dominant disease[6].
  • hypotrichosis 3's genetic association is recorded as KRT74[7].
  • hypotrichosis 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110700[8].
  • hypotrichosis 3's exact match is recorded as http://identifiers.org/doid/DOID:0110700[9].
  • hypotrichosis 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].

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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). hypotrichosis 3. Retrieved May 3, 2026, from https://4ort.xyz/entity/hypotrichosis-3
MLA “hypotrichosis 3.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hypotrichosis-3.
BibTeX @misc{4ortxyz_hypotrichosis-3_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hypotrichosis 3}}, year = {2026}, url = {https://4ort.xyz/entity/hypotrichosis-3}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hypotrichosis 3 — https://4ort.xyz/entity/hypotrichosis-3 (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. 6w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo id MONDO_0013514
    Imported from
    Umls cui C3151432
    Disease ontology id DOID:0110700
    + 8 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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