FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term restrictive cardiomyopathy ID (Ontology) DOID:397 (Human Disease)
Definition An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.
Also Known As "Cardiomyopathy, constrictive" ; "primary restrictive cardiomyopathy"
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 restrictive cardiomyopathy       4      3      1
 for disease ribbon | restrictive cardiomyopathy       --       1       --
 model of | restrictive cardiomyopathy       2      1       --
 DOES NOT model | restrictive cardiomyopathy       3       --       --
Spanning Tree (Parents/Children)
Only view relationship: 
  cardiomyopathy
   |__intrinsic cardiomyopathy
       |__restrictive cardiomyopathy  12 rec.
           |__endomyocardial fibrosis
           |__familial restrictive cardiomyopathy 1 2 rec.
           |__familial restrictive cardiomyopathy 2
           |__familial restrictive cardiomyopathy 3 2 rec.
           |__familial restrictive cardiomyopathy 6 1 rec.
           |__Loeffler endocarditis
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Is a intrinsic cardiomyopathy
Part of
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Synonyms
  • "Cardiomyopathy, constrictive" EXACT
    "Familial restrictive cardiomyopathy" RELATED[ MIM:115210 ]
    "primary restrictive cardiomyopathy" EXACT
Secondary IDs
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ICD10CM:I42.5
MESH:D002313
MIM:115210
MIM:PS115210
NCI:C62798
ORDO:75249
SNOMEDCT_US_2023_03_01:389996009
UMLS_CUI:C0007196