Stereotypic Movement Disorder

Alias:
Stereotypy Habit Disorder
Stereotyped Repetitive Movements
Stereotype Habit Disorder
Stereotyped Disorder
Stereotypes Nos
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Stereotypic Movement Disorder, also known as stereotypy habit disorder, is related to pervasive developmental disorder and autism spectrum disorder, and has symptoms including athetosis, clonus and muscular fasciculation. An important gene associated with Stereotypic Movement Disorder is MECP2 (Methyl-CpG Binding Protein 2), and among its related pathways/superpathways are Rett syndrome causing genes and Antipsychotics Pathway (Metabolic Side Effects), Pharmacodynamics. Affiliated tissues include eye and skin, and related phenotypes are nervous system and embryo
Related ID:
MESH:D019956
ICD11:1111628448

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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37
343
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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