Parkinson Disease 1, Autosomal Dominant (PARK1)

Alias:
Autosomal Dominant Parkinson Disease 1
Atypical Parkinson Disease
Parkinson's Disease 1
Parkinson Disease 1
Park1
Parkinson Disease 1, Autosomal Dominant Lewy Body
Autosomal Dominant Parkinson's Disease 1
Parkinson Disease Autosomal Dominant 1
Parkinson Disease, Familial, Type 1
Parkinson Disease Familial Type 1
Parkinson Disease, Type 1
Lewy Body Parkinsonism
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Parkinson Disease 1, Autosomal Dominant, also known as autosomal dominant parkinson disease 1, is related to kufor-rakeb syndrome and multiple system atrophy 1, and has symptoms including muscle rigidity, myoclonus and sleep disturbances. An important gene associated with Parkinson Disease 1, Autosomal Dominant is SNCA (Synuclein Alpha), and among its related pathways/superpathways are Neuroscience and Parkinson's disease pathway. The drugs Dopamine and Levodopa have been mentioned in the context of this disorder. Affiliated tissues include brain and subthalamic nucleus, and related phenotypes are loss of ambulation and rigidity
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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5
66
67

Medical Symptom

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

Gene & Mutation

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Mutations
No data available

Related Drugs

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Status
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No data available

Disease Model

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

References Literature

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