Movement Disease

Alias:
Movement Disorders
Movement Disorder
Abnormality of Movement
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Movement Disease, also known as movement disorders, is related to tremor and huntington disease, and has symptoms including ataxia, athetosis and back pain. An important gene associated with Movement Disease is BCS1L (BCS1 Homolog, Ubiquinol-Cytochrome C Reductase Complex Chaperone), and among its related pathways/superpathways are Neuroscience and Alpha-synuclein signaling. The drugs Iron and Cysteine have been mentioned in the context of this disorder. Affiliated tissues include brain and spinal cord, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D009069
ICD11:1462849226

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
117
1641
4

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top