Parkinson Disease 3, Autosomal Dominant (PARK3)

Alias:
Parkinson Disease 3
Park3
Parkinson Disease 3, Autosomal Dominant Lewy Body
Parkinson's Disease 3
Autosomal Dominant Lewy Body Parkinson Disease 3
Autosomal Dominant Parkinson Disease 3
Parkinson Disease, Familial, Type 1
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Parkinson Disease 3, Autosomal Dominant, also known as parkinson disease 3, is related to tremor and parkinsonism. An important gene associated with Parkinson Disease 3, Autosomal Dominant is PARK3 (Parkinson Disease 3 (Autosomal Dominant, Lewy Body)), and among its related pathways/superpathways are Neuroscience and Alpha-synuclein signaling. Affiliated tissues include subthalamic nucleus and brain, and related phenotypes are homeostasis/metabolism and nervous system

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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14
174
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Medical Symptom

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Description
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No data available

Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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