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This is a non-core endpoint: only basic statistics are computed.

See these related core endpoints for full statistics:

Abnormalities of gait and mobility

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.

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Endpoint definition

Endpoint definition steps

FinnGen

Phenotype data

473681

1. Apply sex-specific rule

None

473681

2. Check conditions

None

473681

3. Check pre-conditions, main-only, mode, registry filters

Registry filters:

  • Hospital discharge: ICD-10 R26
  • Cause of death: ICD-10 R26

2 out of 7 registries used, show all original rules.

4029

4. Check minimum number of events

None

4029

5. Include endpoints

None

4029

6. Filter based on genotype QC (FinnGen only)

3876

Control definitions (FinnGen only)

Extra metadata

Level in the ICD hierarchy 3
Special GAITCHANGE
First used in FinnGen datafreeze DF4
Parent code in ICD-10 R25-R29
Name in latin Abnormitates incessus et mobilitatis

Case counts by codes

FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

-FinRegistry-

This endpoint is excluded from FinRegistry analyses (omitted endpoint).

-FinnGen-

Key figures

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

-FinnGen-

Age distribution of first events

-FinnGen-

Year distribution of first events

-FinnGen-

Cumulative Incidence Function

Not a core endpoint, no data to show.

Mortality – FinRegistry

This endpoint is excluded from FinRegistry analyses (omitted endpoint).

Relationships between endpoints

Index endpoint: R18_ABNORMALITI_GAIT_MOBIL – Abnormalities of gait and mobility

GWS hits: -

This endpoint is excluded from FinRegistry analyses (omitted endpoint).