Trismus Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Limitation in the ability to open the mouth. (Human Phenotype Ontology, HP_0000211)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014313
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Genes

4 genes/proteins associated with the disease Trismus from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
BCHE butyrylcholinesterase 2.88009
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 1.24843
FOS FBJ murine osteosarcoma viral oncogene homolog 1.03678
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.01212