Multiple System Atrophy 1 (MSA1)

Alias:
Multiple System Atrophy
Shy-Drager Syndrome
Multiple System Atrophy 1, Susceptibility to
Multisystem Atrophy
Msa
Sporadic Olivopontocerebellar Atrophy
Msa1
Progressive Autonomic Failure with Multiple System Atrophy
Multiple System Atrophy, Susceptibility to
Multisystem Atrophy, Susc.to, Type 1
Msa1, Susceptibility to
Opca
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Multiple System Atrophy 1, also known as multiple system atrophy, is related to orthostatic hypotension and pure autonomic failure. An important gene associated with Multiple System Atrophy 1 is COQ2 (Coenzyme Q2, Polyprenyltransferase), and among its related pathways/superpathways are Neuroscience and 5q35 copy number variation. The drugs Acetylcholine and Zoledronic acid have been mentioned in the context of this disorder. Affiliated tissues include Limb, Bone and brain, and related phenotypes are abnormal pyramidal sign and dysarthria
Related ID:
MESH:D012791
ICD11:1890931931

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
1-9/100000
34
591
26

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
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