ONTOLOGY REPORT - ANNOTATIONS
Term: Cardiomyopathy, Restrictive
Accession: RDO:0005133
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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
Cardiomyopathy, Restrictive
G
Ctgf
connective tissue growth factor
IEP
1
21,327,099
21,330,215
RGD:2314513
RGD
G
Des
desmin
ISS
9
74,637,783
74,645,499
RGD:1580290
RGD
G
Map2k6
mitogen-activated protein kinase kinase 6
Model
ISS
10
99,859,684
99,974,446
RGD:1302548
RGD
G
Mybpc3
myosin binding protein C, cardiac
ISS
3
75,478,579
75,496,750
RGD:1580232
RGD
G
Prkcd
protein kinase C, delta
IEP
16
5,954,218
5,975,743
RGD:1642535
RGD
G
Sod2
superoxide dismutase 2, mitochondrial
ISS
1
41,862,997
41,870,327
RGD:1580836
RGD
G
Tnni3
troponin I type 3 (cardiac)
ISS
1
68,028,198
68,031,882
RGD:1580419
RGD
G
Tnnt2
troponin T type 2 (cardiac)
ISS
13
48,872,972
48,885,815
RGD:1580232
RGD
G
Wrn
Werner syndrome, RecQ helicase-like
ISS
16
62,535,144
62,668,700
RGD:1580820
RGD
Cardiomyopathy, Familial Restrictive, 1
G
Tnni3
troponin I type 3 (cardiac)
ISS
1
68,028,198
68,031,882
RGD:7240710
OMIM
Cardiomyopathy, Familial Restrictive, 3
G
Tnnt2
troponin T type 2 (cardiac)
ISS
13
48,872,972
48,885,815
RGD:7240710
OMIM
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