hypertrophic cardiomyopathy 16

Summary
Synonym
  • CMH16
  • cardiomyopathy familial hypertrophic 16
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110322
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
59006 Myoz2 myozenin 2

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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: December 9, 2024