Parkinson's disease, strict definition

Description

secondary Parkinson disease: Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42)

Data source
FinnGen phenocode PDSTRICT
Hospital Discharge registry ICD-10: G20, ICD-9: 3320A, ICD-8: 34200
Cause of Death registry ICD-10: G20, ICD-9: 3320A, ICD-8: 34200
KELA reimboursements codes 110
KELA reimbursements ICD-10: G20
First defined in version DF2
Ontology
DOID 13548
GWAS catalog 1001175
MESH D010300
SNOMED CT 265377002

Key figures

Sex All Female Male
Number of individuals 1495 697 798
Unadjusted prevalence (%) 0.86 0.7 1.06
Mean age at first event (years) 67.91 67.66 68.12
Case fatality at 5-years (%) 11.71 10.62 12.66

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 6 5 6
Recurrence at 6 months (%) 69.68 66.52 72.43

Associations

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