MYH9-related disorder

blood platelet disease that has material basis in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract
MedicalCondition class_of_disease Q3843790
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MYH9-related disorder

Summary

MYH9-related disorder is a class of disease[1].

Key Facts

  • MYH9-related disorder's instance of is recorded as class of disease[2].
  • MYH9-related disorder is a type of blood platelet disease[3].
  • MYH9-related disorder is a type of Inherited giant platelet disorder[4].
  • MYH9-related disorder's genetic association is recorded as MYH9[5].
  • MYH9-related disorder's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060651[6].
  • MYH9-related disorder's exact match is recorded as http://identifiers.org/doid/DOID:0060651[7].
  • MYH9-related disorder's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_182050[8].
  • MYH9-related disorder's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].

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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). MYH9-related disorder. Retrieved May 3, 2026, from https://4ort.xyz/entity/myh9-related-disorder
MLA “MYH9-related disorder.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/myh9-related-disorder.
BibTeX @misc{4ortxyz_myh9-related-disorder_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{MYH9-related disorder}}, year = {2026}, url = {https://4ort.xyz/entity/myh9-related-disorder}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): MYH9-related disorder — https://4ort.xyz/entity/myh9-related-disorder (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. 7w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Icd-11 id (foundation) 109013938
    On focus list of wikimedia project WikiProject Medicine
    Gard rare disease id 180
    Imported from
    + 14 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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