Parkinson Disease 5, Autosomal Dominant (PARK5)

Alias:

Parkinson Disease 5, Autosomal Dominant, Susceptibility to

Parkinson Disease 5

Parkinson Disease 5, Susceptibility to

Park5

Parkinson Disease Autosomal Dominant 5

Parkinson Disease, Type 5

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Parkinson Disease 5, Autosomal Dominant, is also known as parkinson disease 5. An important gene associated with Parkinson Disease 5, Autosomal Dominant is UCHL1 (Ubiquitin C-Terminal Hydrolase L1). Affiliated tissues include thalamus and brain, and related phenotypes are rigidity and postural instability

Related ID：

MALACARDS：PRK098

OMIM：613643

MESH：D010300