≡ Risteys
R9

Documentation Changelog GitHub Contact & Feedback

Other osteochondrodysplasias

DOID EFO MESH SNOMED PheWeb

Q17_OTHER_OSTEOCHONDROD

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

Endpoint definition

↥
FinnGen phenotype data

392423 individuals

diagram downward connector

Apply sex-specific rule None

392423

diagram downward connector

Check conditions None

392423

diagram downward connector
diagram bullet

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.

223

diagram downward connector

Check minimum number of events None

223

diagram downward connector

Include endpoints None

223

diagram downward connector
diagram bullet diagram downward connector

Remove individuals based on genotype QC

213

diagram downward connector
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

↥

Key figures

All Female Male
Number of individuals 213 139 74
Unadjusted prevalence (%) 0.06 0.07 0.04
Mean age at first event (years) 33.85 34.85 31.97

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

↥

Index endpoint: Q17_OTHER_OSTEOCHONDROD – Other osteochondrodysplasias
GWS hits: 2

Survival analyses between endpoints

↥

Plot

before Other osteochondrodysplasias
after Other osteochondrodysplasias

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Other osteochondrodysplasias

↥

Endpoint not on priority list, no data to show.