Hereditary sideroblastic anaemia


anemia (phenotype): ['A reduction in the number of circulating erythrocytes or in the quantity of hemoglobin.']

Endpoint definition

FinnGen phenotype data

321302 individuals

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Apply sex-specific rule None


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Check conditions None


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Filter registries

Hospital Discharge: ICD-10 D64.0
Hospital discharge: ICD-9 2850A
Hospital discharge: ICD-8 $!$
Cause of death: ICD-10 D64.0
Cause of death: ICD-9 2850A
Cause of death: ICD-8 $!$


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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9


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Check minimum number of events None


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Include endpoints None


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Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 D64
Name in latin Anaemia sideroblastica hereditaria

Summary Statistics

Key figures

All Female Male
Number of individuals 82 39 43
Unadjusted prevalence (%) 0.03 0.02 0.03
Mean age at first event (years) 64.96 60.93 68.61


Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence


Index endpoint: D3_SIDEROANAEMIAHERED – Hereditary sideroblastic anaemia
GWS hits:

Survival analyses between endpoints


before Hereditary sideroblastic anaemia
after Hereditary sideroblastic anaemia

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Drugs most likely to be purchased after Hereditary sideroblastic anaemia