tic disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that is characterized by the persistent presence of involuntary brief movements or sounds occuring intermittently and unpredictably out of a background of normal motor activity. (Human Disease Ontology, DOID_2769)
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7 genes associated with the disease tic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
COL27A1 collagen, type XXVII, alpha 1 0.464771
LINC00587 long intergenic non-protein coding RNA 587 0.100789
POLR3B polymerase (RNA) III (DNA directed) polypeptide B 0.080593
PHEX phosphate regulating endopeptidase homolog, X-linked 0.080593
THSD7A thrombospondin, type I, domain containing 7A 0.080593
HDGFL1 hepatoma derived growth factor-like 1 0.052255
PICALM phosphatidylinositol binding clathrin assembly protein 0.043246