restrictive cardiomyopathy

Summary
Synonym
  • Cardiomyopathy, constrictive
  • primary restrictive cardiomyopathy
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.
Super Class
intrinsic cardiomyopathy
Disease Ontology
DOID:397
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
84665 MYPN myopalladin
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description Source
13346 Des desmin
17879 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult
17882 Myh2 myosin, heavy polypeptide 2, skeletal muscle, adult
17883 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic
17884 Myh4 myosin, heavy polypeptide 4, skeletal muscle
17888 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha
21954 Tnni3 troponin I, cardiac 3
22427 Wrn Werner syndrome RecQ like helicase
26397 Map2k3 mitogen-activated protein kinase kinase 3
68802 Mypn myopalladin
Displaying all 3 entries
Gene ID Gene Symbol Description Source
24837 Tnnt2 troponin T2, cardiac type
29248 Tnni3 troponin I3, cardiac type
170538 Prkcd protein kinase C, delta
Displaying 1 entry
Gene ID Gene Symbol Description Source
853313 PBS2 mitogen-activated protein kinase kinase PBS2

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