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Standards Ontologies Notations
familial hypertrophic cardiomyopathy

Summary
Definition
A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.
Super Class
hypertrophic cardiomyopathy
External Links
Disease Ontology
DOID:0080326
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
Related Genes
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
668940 Myh7b myosin, heavy chain 7B, cardiac muscle, beta
Displaying all 5 entries
Gene ID Gene Symbol Description Source
24837 Tnnt2 troponin T2, cardiac type
24851 Tpm1 tropomyosin 1
289596 Corin corin, serine peptidase
295929 Mybpc3 myosin binding protein C3
363925 Myl2 myosin light chain 2
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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: August 19, 2024