Parkinson Disease 8, Autosomal Dominant (PARK8)

Alias:
Autosomal Dominant Parkinson Disease 8
Parkinson Disease 8
Parkinson's Disease 8
Park8
Parkinson Disease, Type 8, Autosomal Dominant
Autosomal Dominant Parkinson's Disease 8
Parkinson Disease-8
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Parkinson Disease 8, Autosomal Dominant, also known as autosomal dominant parkinson disease 8, is related to early-onset parkinson's disease and parkinsonism, and has symptoms including muscle rigidity, bradykinesia and resting tremor. An important gene associated with Parkinson Disease 8, Autosomal Dominant is LRRK2 (Leucine Rich Repeat Kinase 2), and among its related pathways/superpathways are Signal Transduction and GDNF signaling. Affiliated tissues include subthalamic nucleus and olfactory bulb, and related phenotypes are hyposmia and dementia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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20
257
102

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
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References Literature

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