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Disease Info Card
Stereotypic Movement Disorder
Information about Stereotypic Movement Disorder: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Stereotypic Movement Disorder
Most recent studies have shown that Stereotypic Movement Disorder shares some biological mechanisms with anxiety-disorders, autism-spectrum-disorders, autistic-disorder, catalepsy, depressive-disorder, developmental-disabilities, dyskinetic-syndrome, lingual-facial-buccal-dyskinesia, mental-disorders, movement-disorders, nervousness, parkinson-disease, pcp---hallucinogen-related-disorder, psychotic-disorders, schizophrenia, stereotyped-behavior.
Among the many pathways, these few ones have gauged particular interests from scientists studying Stereotypic Movement Disorder, and have been seen in publications frequently: Cognition, Dopamine Uptake, Grooming Behavior, Habituation, Hypersensitivity, Innervation, Locomotion, Pathogenesis, Prepulse Inhibition, Reflex, Response To Amphetamine, Response To Cocaine, Secretion, Sensitization, Social Behavior, Startle Response, Swimming, Thigmotaxis, Transport
Quite a number of genes have been found to play important roles in Stereotypic Movement Disorder, such as AGT, AMPH, BBS9, CAT, CCK, DIO2, DRD1, DRD2, DRD3, ERMAP, FOS, LMOD1, NF2, POMC, PRL, SLC6A3, TH. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.