hyperCKmia

human disease
MedicalCondition rare_disease Q54366429
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hyperCKmia

Summary

hyperCKmia is a rare disease[1].

Key Facts

  • hyperCKmia's instance of is recorded as rare disease[2].
  • hyperCKmia's instance of is recorded as class of disease[3].
  • hyperCKmia is a type of genetic disease[4].
  • hyperCKmia is a type of autosomal dominant disease[5].
  • hyperCKmia is a type of inherited metabolic disorder[6].
  • hyperCKmia's medical examination is recorded as serum creatine kinase level[7].
  • hyperCKmia's has characteristic is recorded as abnormally high value[8].
  • hyperCKmia's NCI Thesaurus ID is recorded as C148327[9].
  • hyperCKmia's genetic association is recorded as CAV3[10].
  • hyperCKmia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111338[11].
  • hyperCKmia's exact match is recorded as http://identifiers.org/doid/DOID:0111338[12].

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APA 4ort.xyz Knowledge Graph. (2026). hyperCKmia. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyperckmia
MLA “hyperCKmia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyperckmia.
BibTeX @misc{4ortxyz_hyperckmia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyperCKmia}}, year = {2026}, url = {https://4ort.xyz/entity/hyperckmia}, note = {Accessed: 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. 17d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo id MONDO_0007402
    Imported from
    Medical examination serum creatine kinase level
    Nci thesaurus id C148327
    + 11 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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