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