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Standards Ontologies Notations
hypertrophic cardiomyopathy 1

Summary
Synonym
  • CMH1
  • cardiomyopathy, familial hypertrophic 1
  • hypertrophic cardiomyopathy 19
Definition
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.
Super Class
familial hypertrophic cardiomyopathy
Disease Ontology
DOID:0110307
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4625 MYH7 myosin heavy chain 7
Displaying 1 entry
Gene ID Gene Symbol Description Source
140781 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta
Displaying 1 entry
Gene ID Gene Symbol Description Source
36002 sqa spaghetti-squash activator
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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