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
- Familial Parkinson disease
- Other genetic Parkinsonism
- Autosomal dominant familial Parkinson disease
- Parkinson disease LRRK2 gene mutation 12p11.23-q13.11
- PARK8
- Parkinson disease synuclein gene mutation 4q21.23
- PARK1
- Parkinson disease synduclein duplications or triplications
- Parkinson disease UCHL-1 gene mutations 4p14
- PARK5
- Autosomal recessive familial Parkinson disease
- Parkinson disease parkin mutations
- PARK 2
- Parkinson disease DJ-1 gene mutations 1p36
- PARK 7
- Parkinson disease PINK gene mutations
- PARK 6
- PINK 1
- Parkinson disease ATP13A2 mutations
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