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

See these related core endpoints for full statistics:

Amyloidosis

E4_AMYLOIDOSIS

amyloidosis: A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.

Endpoint definition

FinnGen phenotype data

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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

Hospital Discharge: ICD-10 E85
Cause of death: ICD-10 E85

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

499

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Check minimum number of events None

499

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Remove individuals based on genotype QC

500

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E4_AMYLOIDOSIS

Control definitions

Control exclude E4_METABOLIA

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 E70-E90
Name in latin Amyloidosis

Similar endpoints

List of similar endpoints to Amyloidosis based on the number of shared cases.

Venn diagram with an highlighted set fully inside another set Broader endpoints:

Venn diagram with a set fully inside an highlighted set Narrower endpoints:

Show all endpoint correlations

Summary Statistics

Key figures

All Female Male
Number of individuals 500 244 256
Unadjusted prevalence (%) 0.13 0.12 0.15
Mean age at first event (years) 62.60 58.59 66.42

Mortality

Not a core endpoint, no data to show.

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Not a core endpoint, no data to show.

Correlations

Index endpoint: E4_AMYLOIDOSIS – Amyloidosis
GWS hits:

Survival analyses between endpoints

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Amyloidosis

Endpoint not on priority list, no data to show.