This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
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This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
R18_ABNORMALITI_GAIT_MOBIL
gait apraxia: Impaired ambulation not attributed to sensory impairment or motor weakness. frontal lobe disorders; basal ganglia diseases (e.g., parkinsonian disorders); dementia, multi-infarct; alzheimer disease; and other conditions may be associated with gait apraxia.
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
473681 |
1. Apply sex-specific ruleNone |
473681 |
2. Check conditionsNone |
473681 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters: 2 out of 7 registries used, show all original rules. |
4029 |
4. Check minimum number of eventsNone |
4029 |
5. Include endpointsNone |
4029 |
6. Filter based on genotype QC (FinnGen only) |
3876 |
Control definitions (FinnGen only)
Extra metadata
List of similar endpoints to
Abnormalities of gait and mobility
based on the number of shared cases.
Similar with more cases:
Similar with less cases:
None
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
All | Female | Male | |
---|---|---|---|
Number of individuals | 3876 | 1795 | 2081 |
Unadjusted period prevalence (%) | 0.89 | 0.70 | 1.05 |
Median age at first event (years) | 68.18 | 65.18 | 70.77 |
Not a core endpoint, no data to show.
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
Index endpoint: R18_ABNORMALITI_GAIT_MOBIL – Abnormalities of gait and mobility
GWS hits: -
This endpoint is excluded from FinRegistry analyses (omitted endpoint).