asymmetric septal hypertrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. (Human Phenotype Ontology, HP_0001670)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001670
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Genes

10 genes associated with the asymmetric septal hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CALR3 calreticulin 3
CAV3 caveolin 3
GNS glucosamine (N-acetyl)-6-sulfatase
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYLK2 myosin light chain kinase 2
MYOZ2 myozenin 2
NAGLU N-acetylglucosaminidase, alpha
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
SGSH N-sulfoglucosamine sulfohydrolase