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

See these related core endpoints for full statistics:

Motor neuron disease (with DMD)

DOID Endpoint Browser

MND

muscular disease: Acquired, familial, and congenital disorders of skeletal muscle and smooth muscle.

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Endpoint definition

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Endpoint definition steps

FinnGen

Phenotype data

429209

1. Apply sex-specific rule

None

429209

2. Check conditions

None

429209

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

Registry filters:

  • Hospital discharge: ICD-10 — G71.06
  • Cause of death: ICD-10 — G71.06

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

26

4. Check minimum number of events

None

26

5. Include endpoints

571

6. Filter based on genotype QC (FinnGen only)

555

Control definitions (FinnGen only)

Control exclude F5_PSYCH, NEURODIS

Extra metadata

First used in FinnGen datafreeze DF3
Parent code in ICD-10 G710
Name in latin Dystrophia musculorum gravis (Duchenne)

Case counts by codes

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FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

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-FinRegistry-

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

-FinnGen-

Key figures

All Female Male
Number of individuals 555 210 345
Unadjusted period prevalence (%) 0.15 0.09 0.19
Median age at first event (years) 66.75 66.94 66.64

-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

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

Relationships between endpoints

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Index endpoint: MND – Motor neuron disease (with DMD)

GWS hits: -

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