hypertrophic cardiomyopathy 20

Summary
Synonym
  • CMH20
  • cardiomyopathy familial hypertrophic 20
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
Super Class
familial hypertrophic cardiomyopathy
External Links
Disease Ontology
DOID:0110326
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
91624 NEXN nexilin F-actin binding protein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024