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congenital myopathy

human disease
MedicalCondition designated_intractable_rare_disease Q112412
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congenital myopathy

Summary

congenital myopathy is a designated intractable/rare disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • congenital myopathy's instance of is recorded as designated intractable/rare disease[3].
  • congenital myopathy's instance of is recorded as class of disease[4].
  • congenital myopathy is a type of muscular disease[5].
  • congenital myopathy is a type of congenital disorder[6].
  • congenital myopathy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4726[7].
  • congenital myopathy's health specialty is recorded as neurology[8].
  • congenital myopathy's genetic association is recorded as HACD1[9].
  • congenital myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080100[10].
  • congenital myopathy's exact match is recorded as http://identifiers.org/doid/DOID:0080100[11].
  • congenital myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97245[12].
  • congenital myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].

Why It Matters

congenital myopathy has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Related Entities

neurology

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . nanbyou.or.jp. Retrieved . nanbyou.or.jp. Provenance: wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.

📑 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). congenital myopathy. Retrieved May 3, 2026, from https://4ort.xyz/entity/congenital-myopathy
MLA “congenital myopathy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/congenital-myopathy.
BibTeX @misc{4ortxyz_congenital-myopathy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{congenital myopathy}}, year = {2026}, url = {https://4ort.xyz/entity/congenital-myopathy}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): congenital myopathy — https://4ort.xyz/entity/congenital-myopathy (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/congenital-myopathy · Last refreshed:

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. 5w ago · Jindřich Rubeš · 2026-06-11 view diff on Wikidata ↗
    Instance of → —
    Svkkl authority id → 0211523-vrozene-myopatie
    Genetic association → HACD1
    Instance of → designated intractable/rare disease, class of disease
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbcreateclaim-create:1| */ [[Property:P9322]]: 0211523-vrozene-myopatie, [[:toollabs:quickstatements/#/batch/259487|batch #259487]]"
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