FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypertrophic cardiomyopathy 20 ID (Ontology) DOID:0110326 (Human Disease)
Definition A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
Also Known As "cardiomyopathy familial hypertrophic 20" ; "CMH20"
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  hypertrophic cardiomyopathy
   |__familial hypertrophic cardiomyopathy
       |__hypertrophic cardiomyopathy 20
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Is a familial hypertrophic cardiomyopathy
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Synonyms
  • "cardiomyopathy familial hypertrophic 20" EXACT
    "CMH20" EXACT OMO:0003012
Secondary IDs
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MIM:613876