FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial hypertrophic cardiomyopathy ID (Ontology) DOID:0080326 (Human Disease)
Definition A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       3
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 familial hypertrophic cardiomyopathy       4      1
 model of | familial hypertrophic cardiomyopathy       4       --
Spanning Tree (Parents/Children)
Only view relationship: 
  intrinsic cardiomyopathy
   |__hypertrophic cardiomyopathy
       |__familial hypertrophic cardiomyopathy  53 rec.
           |__hypertrophic cardiomyopathy 1 3 rec.
           |__hypertrophic cardiomyopathy 2 2 rec.
           |__hypertrophic cardiomyopathy 3 3 rec.
           |__hypertrophic cardiomyopathy 4 2 rec.
           |__hypertrophic cardiomyopathy 6 1 rec.
           |__hypertrophic cardiomyopathy 7 2 rec.
           |__hypertrophic cardiomyopathy 8 1 rec.
           |__hypertrophic cardiomyopathy 9 3 rec.
           |__hypertrophic cardiomyopathy 10 9 rec.
           |__hypertrophic cardiomyopathy 11 12 rec.
           |__hypertrophic cardiomyopathy 12 2 rec.
           |__hypertrophic cardiomyopathy 13
           |__hypertrophic cardiomyopathy 14 2 rec.
           |__hypertrophic cardiomyopathy 15 2 rec.
           |__hypertrophic cardiomyopathy 16
           |__hypertrophic cardiomyopathy 17 2 rec.
           |__hypertrophic cardiomyopathy 18 1 rec.
           |__hypertrophic cardiomyopathy 20
           |__hypertrophic cardiomyopathy 21
           |__hypertrophic cardiomyopathy 25
           |__hypertrophic cardiomyopathy 26 3 rec.
           |__hypertrophic cardiomyopathy 27
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MESH:D024741
MIM:PS192600
NCI:C84773
ORDO:217569
SNOMEDCT_US_2023_03_01:83978005
UMLS_CUI:C0949658