Cardiomyopathy, Familial Hypertrophic, 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C566005
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Genes

7 genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MYLK2 myosin light chain kinase 2 2.88009
ACTC1 actin, alpha, cardiac muscle 1 2.88009
CAV3 caveolin 3 2.88009
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 2.88009
TNNC1 troponin C type 1 (slow) 2.88009
MYH6 myosin, heavy chain 6, cardiac muscle, alpha 2.88009
MYH7 myosin, heavy chain 7, cardiac muscle, beta 2.88009