stereotypic movement disorder Gene Set

Dataset	DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A specific developmental disorder that is characterized by repeated, rhythmic, purposeless movements or activities such as head banging, nail biting, or body rocking. (Human Disease Ontology, DOID_2303)
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Genes

6 genes co-occuring with the disease stereotypic movement disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
SLITRK1	SLIT and NTRK-like family, member 1	1.85638
ABCB6	ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)	1.33021
MECP2	methyl CpG binding protein 2	0.743547
CCK	cholecystokinin	0.622183
NPY	neuropeptide Y	0.618268
TAC1	tachykinin, precursor 1	0.470711