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 entries 41 - 50 of 56 in total
Gene ID Gene Symbol Description Source
6783 SULT1E1 sulfotransferase family 1E member 1
7167 TPI1 triosephosphate isomerase 1
7941 PLA2G7 phospholipase A2 group VII
8802 SUCLG1 succinate-CoA ligase GDP/ADP-forming subunit alpha
8972 MGAM maltase-glucoamylase
9197 SLC33A1 solute carrier family 33 member 1
10555 AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
23417 MLYCD malonyl-CoA decarboxylase
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
55750 AGK acylglycerol kinase

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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