ONTOLOGY REPORT - ANNOTATIONS


Term:Cardiomyopathy, Restrictive
go back to main search page
Accession:RDO:0005133 term browser browse the term
Definition:A form of CARDIAC MUSCLE disease in which the ventricular walls are excessively rigid, impeding ventricular filling. It is marked by reduced diastolic volume of either or both ventricles but normal or nearly normal systolic function. It may be idiopathic or associated with other diseases (ENDOMYOCARDIAL FIBROSIS or AMYLOIDOSIS) causing interstitial fibrosis.
Synonyms:exact_synonym: Restrictive Cardiomyopathies
 primary_id: MESH:D002313


  • Rat
  • Mouse
  • Human
  • All
  • show annotations for term's descendants
  •     Sort by:
Cardiomyopathy, Restrictive term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Ctgf connective tissue growth factor GBrowse link IEP 1 21,327,099 21,330,215 RGD:2314513 RGD
G Des desmin GBrowse link ISS 9 74,637,783 74,645,499 RGD:1580290 RGD
G Map2k6 mitogen-activated protein kinase kinase 6 GBrowse link Model ISS 10 99,859,684 99,974,446 RGD:1302548 RGD
G Mybpc3 myosin binding protein C, cardiac GBrowse link ISS 3 75,478,579 75,496,750 RGD:1580232 RGD
G Prkcd protein kinase C, delta GBrowse link IEP 16 5,954,218 5,975,743 RGD:1642535 RGD
G Sod2 superoxide dismutase 2, mitochondrial GBrowse link ISS 1 41,862,997 41,870,327 RGD:1580836 RGD
G Tnni3 troponin I type 3 (cardiac) GBrowse link ISS 1 68,028,198 68,031,882 RGD:1580419 RGD
G Tnnt2 troponin T type 2 (cardiac) GBrowse link ISS 13 48,872,972 48,885,815 RGD:1580232 RGD
G Wrn Werner syndrome, RecQ helicase-like GBrowse link ISS 16 62,535,144 62,668,700 RGD:1580820 RGD
Cardiomyopathy, Familial Restrictive, 1 term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Tnni3 troponin I type 3 (cardiac) GBrowse link ISS 1 68,028,198 68,031,882 RGD:7240710 OMIM
Cardiomyopathy, Familial Restrictive, 3 term browser
Symbol Object Name GBrowse Qualifiers Evidence Chr Start Stop Reference Source
G Tnnt2 troponin T type 2 (cardiac) GBrowse link ISS 13 48,872,972 48,885,815 RGD:7240710 OMIM

Term paths to the root
Path 1
Term Annotations click to browse term
  Diseases 30466
    Cardiovascular Diseases 5252
      Heart Diseases 1974
        Cardiomyopathies 491
          Cardiomyopathy, Restrictive 11
            Cardiomyopathy, Familial Restrictive, 1 1
            Cardiomyopathy, Familial Restrictive, 2 0
            Cardiomyopathy, Familial Restrictive, 3 1
paths to the root