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Compton-North congenital myopathy

Human disease
MedicalCondition rare_disease Q21505528
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Summary

Compton-North congenital myopathy is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: congenital myopathy[4]
  • Prevalence: 0.000001[5]
  • Genetic association: CNTN1[6]
  • Age of onset: congenital onset[7], neonatal onset[8]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0080101[9], http://identifiers.org/doid/DOID:0080101[10], http://www.orpha.net/ORDO/Orphanet_210163[11]
  • On focus list of Wikimedia project: WikiProject Medicine[12]
  • P14914: D210163[13]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . Retrieved . wikidata.org.
  4. [6] ↑ . UniProt. Retrieved . wikidata.org.
  5. [7] ↑ . Retrieved . wikidata.org.
  6. [8] ↑ . Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata aliases. 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). Compton-North congenital myopathy. Retrieved October 27, 2026, from https://4ort.xyz/entity/compton-north-congenital-myopathy
MLA “Compton-North congenital myopathy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 27 Oct. 2026, https://4ort.xyz/entity/compton-north-congenital-myopathy.
BibTeX @misc{4ortxyz_compton-north-congenital-myopathy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Compton-North congenital myopathy}}, year = {2026}, url = {https://4ort.xyz/entity/compton-north-congenital-myopathy}, note = {Accessed: 2026-10-27}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Compton-North congenital myopathy — https://4ort.xyz/entity/compton-north-congenital-myopathy (retrieved 2026-10-27)

Canonical URL: https://4ort.xyz/entity/compton-north-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. 4d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Uniprot disease id → DI-01385
    Mesh descriptor id → C567261
    Mondo id → MONDO_0012929
    Instance of → rare disease, class of disease
    + 17 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
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