Parkinson Disease 13, Autosomal Dominant (PARK13)

Alias:

Parkinson Disease 13

Parkinson Disease 13, Autosomal Dominant, Susceptibility to

Park13

Parkinson Disease, Type 13

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Parkinson Disease 13, Autosomal Dominant, also known as parkinson disease 13, is related to parkinson disease, late-onset and movement disease. An important gene associated with Parkinson Disease 13, Autosomal Dominant is HTRA2 (HtrA Serine Peptidase 2). Affiliated tissues include brain, and related phenotypes are tremor and rigidity

Related ID：

MALACARDS：PRK096

OMIM：610297

MESH：D010300