This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
Motor neuron disease (with DMD)
MND
muscular disease: Acquired, familial, and congenital disorders of skeletal muscle and smooth muscle.
Endpoint definition
↥
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. |
29 |
4. Check minimum number of eventsNone |
29 |
5. Include endpoints |
632 |
6. Filter based on genotype QC (FinnGen only) |
618 |
Extra metadata
First used in FinnGen datafreeze
DF3
Parent code in ICD-10
G710
Name in latin
Dystrophia musculorum gravis (Duchenne)
Motor neuron disease (with DMD)
based on the number of shared cases.
Similar with more cases:
Similar with less cases:
Summary Statistics
↥-FinRegistry-
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
-FinnGen-
Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 618 | 247 | 371 |
| Unadjusted period prevalence (%) | 0.15 | 0.10 | 0.19 |
| Median age at first event (years) | 66.79 | 67.18 | 66.53 |
-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: MND – Motor neuron disease (with DMD)
GWS hits: -
This endpoint is excluded from FinRegistry analyses (omitted endpoint).