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Standards Ontologies Notations
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 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
140781 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta
544791 Myh13 myosin, heavy polypeptide 13, skeletal muscle
668940 Myh7b myosin, heavy chain 7B, cardiac muscle, beta
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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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024