Familial Parkinson disease (Q41060): Difference between revisions
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Revision as of 07:07, 13 August 2026
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A00.01 |
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| English | Familial Parkinson disease |
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes. |
