FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypertrophic cardiomyopathy 8 ID (Ontology) DOID:0110314 (Human Disease)
Definition A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.
Also Known As "cardiomyopathy hypertrophic mid-left ventricular chamber type 1" ; "cardiomyopathy, familial hypertrophic, 8"
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 Genes
 hypertrophic cardiomyopathy 8       1
 for disease ribbon | hypertrophic cardiomyopathy 8       1
 model of | hypertrophic cardiomyopathy 8       1
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  hypertrophic cardiomyopathy
   |__familial hypertrophic cardiomyopathy
       |__hypertrophic cardiomyopathy 8  1 rec.
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Is a familial hypertrophic cardiomyopathy
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Synonyms
  • "cardiomyopathy hypertrophic mid-left ventricular chamber type 1" EXACT
    "cardiomyopathy, familial hypertrophic, 8" EXACT
Secondary IDs
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MIM:608751