sarcoglycanopathy

collection of diseases resulting from mutations in any of the four sarcoglycan genes
MedicalCondition class_of_disease Q7423586
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sarcoglycanopathy

Summary

sarcoglycanopathy is a class of disease[1].

Key Facts

  • sarcoglycanopathy's instance of is recorded as class of disease[2].
  • sarcoglycanopathy's instance of is recorded as muscular disease[3].
  • sarcoglycanopathy's instance of is recorded as genetic disease[4].
  • sarcoglycanopathy is a type of autosomal recessive limb-girdle muscular dystrophy[5].
  • sarcoglycanopathy is a type of qualitative or quantitative protein defects in neuromuscular diseases[6].
  • sarcoglycanopathy's health specialty is recorded as neurology[7].
  • sarcoglycanopathy's health specialty is recorded as myology[8].
  • sarcoglycanopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_207052[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). sarcoglycanopathy. Retrieved May 3, 2026, from https://4ort.xyz/entity/sarcoglycanopathy
MLA “sarcoglycanopathy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sarcoglycanopathy.
BibTeX @misc{4ortxyz_sarcoglycanopathy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{sarcoglycanopathy}}, year = {2026}, url = {https://4ort.xyz/entity/sarcoglycanopathy}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): sarcoglycanopathy — https://4ort.xyz/entity/sarcoglycanopathy (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. 3d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0016140
    Kegg id H00565
    Orphanet id 207052
    Microsoft academic id (discontinued) 2779561866
    + 9 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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