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Haemolytic disease of fetus and newborn

P16_HAEMOLYTIC_DISEA_FETUS_NEWBO

Endpoint definition

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 P55
  • Cause of death: ICD-10 P55

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

32

4. Check minimum number of events

None

32

5. Include endpoints

None

32

6. Filter based on genotype QC (FinnGen only)

30

Control definitions (FinnGen only)

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF4
Parent code in ICD-10 P[5-6]
Name in latin Morbus haemolyticus fetus sive neonati

Case counts by codes

FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

-FinRegistry-

Key figures

All Female Male
Number of individuals
Whole population 2935 1428 1507
Only index persons 1452 693 759
Unadjusted period prevalence (%)
Whole population 0.04 0.04 0.04
Only index persons 0.03 0.03 0.03
Median age at first event (years)
Whole population - 0.01 0.01
Only index persons 0.00 0.01 0.00

-FinnGen-

Key figures

All Female Male
Number of individuals 30 17 13
Unadjusted period prevalence (%) 0.01 0.01 0.01
Median age at first event (years) 0.02 0.02 0.02

-FinRegistry-

Age distribution of first events

-FinnGen-

Age distribution of first events

-FinRegistry-

Year distribution of first events

-FinnGen-

Year distribution of first events

-FinRegistry-

Cumulative Incidence Function

-FinnGen-

Cumulative Incidence Function

Not a core endpoint, no data to show.

Mortality – FinRegistry

Relationships between endpoints

Index endpoint: P16_HAEMOLYTIC_DISEA_FETUS_NEWBO – Haemolytic disease of fetus and newborn

GWS hits: -

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