8A00.01 Familial Parkinson disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


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.

postcoordination

Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.

Has manifestation  - multiple selections are allowed
Has severity  - only one may be selected

synonyms

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