Athetosis Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Athetosis (from the Greek word for 'changeable' or 'unfixed') refers to an inability to sustain the muscles of the fingers, toes, tongue, or any other group of muscles in a fixed position. Instead, posture is interrupted by slow, purposeless involuntary movements. (Human Phenotype Ontology, HP_0002305)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D001264
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Genes

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

Symbol	Name	Standardized Value
PRL	prolactin	1.58113
DRD2	dopamine receptor D2	1.45352
FOS	FBJ murine osteosarcoma viral oncogene homolog	1.37761
BDNF	brain-derived neurotrophic factor	1.30451
SLC22A2	solute carrier family 22 (organic cation transporter), member 2	1.28487
CYP2C9	cytochrome P450, family 2, subfamily C, polypeptide 9	1.15967
EGR1	early growth response 1	1.08407
CAT	catalase	1.07804
TH	tyrosine hydroxylase	1.05052
CYP3A4	cytochrome P450, family 3, subfamily A, polypeptide 4	1.01025