FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypertrophic cardiomyopathy 4 ID (Ontology) DOID:0110310 (Human Disease)
Definition A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11.
Also Known As "cardiomyopathy, familial hypertrophic, 4" ; "CMH4"
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Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 hypertrophic cardiomyopathy 4       1      1
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  hypertrophic cardiomyopathy
   |__familial hypertrophic cardiomyopathy
       |__hypertrophic cardiomyopathy 4  2 rec.
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Is a familial hypertrophic cardiomyopathy
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Synonyms
  • "cardiomyopathy, familial hypertrophic, 4" EXACT
    "CMH4" EXACT OMO:0003012
Secondary IDs
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MIM:115197