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Other osteochondrodysplasias

DOID EFO MESH SNOMED Endpoint Browser PheWeb

Q17_OTHER_OSTEOCHONDROD

osteochondrodysplasia: A term referring to disorders characterized by abnormalities in the development of bones and cartilage.

Endpoint definition

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FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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

Hospital Discharge: ICD-10 Q78
Cause of death: ICD-10 Q78

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

253

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Check minimum number of events None

253

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Include endpoints None

253

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Remove individuals based on genotype QC

241

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Q17_OTHER_OSTEOCHONDROD

Control definitions

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF4
Parent code in ICD-10 Q6[5-9]|Q7
Name in latin Aliae osteochondrodysplasiae

Summary Statistics

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Key figures

All Female Male
Number of individuals 241 152 89
Unadjusted prevalence (%) 0.06 0.07 0.05
Mean age at first event (years) 34.56 35.87 32.31

Mortality

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

Correlations

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Index endpoint: Q17_OTHER_OSTEOCHONDROD – Other osteochondrodysplasias
GWS hits: 1

Survival analyses between endpoints

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Plot

before Other osteochondrodysplasias
after Other osteochondrodysplasias

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Other osteochondrodysplasias

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Endpoint not on priority list, no data to show.