Version: 0.0.9 | Published: 26 Jul 2023 | Updated: 669 days ago
Summary
DOI Name:
Documentation
Description:
The UK CF Registry is a centralised database of all 60 CF centres across the UK. Data are manually entered in calendar years by CF clinical teams for the 99% of people with a diagnosis of CF who consent to their data being donated to the Registry. Data are entered onto a secure web-portal. For more information please see www.cysticfibrosis.org.uk/registry and 'Data Resource Profile: The UK CF Registry' published in the International Journal of Epidemiology (2018 Feb 1;47(1)9-10e).
Is Part Of:
No Group
Coverage
Spatial:
UK
Typical Age Range:
0-150
Physical Sample Availability:
NOT AVAILABLE
Provenance
Temporal
Accrual Periodicity:
ANNUAL
Distribution Release Date:
01 September 2019
Start Date:
01 January 1996
End Date:
01 September 2019
Accessibility
Access
Access Rights:
Access Request Cost:
Whilst the UK CF Registry does not charge for data, it must recoup costs of data
handling (including extract and cleaning), project management, and analysis
(where applicable) on behalf of third parties. The charging structure outlined
below is designed to be fair, proportionate, and transparent whilst furthering
the Registry’s aim of stimulating research use of the data for the benefit of
people with cystic
fibrosis.https://www.cysticfibrosis.org.uk/the-work-we-do/uk-cf-registry/apply-for-data-from-the-uk-cf-registry
Jurisdictions:
GB
Data Controller:
Cystic Fibrosis Trust
Data Processor:
Cystic Fibrosis Trust
Usage
Resource Creators:
Cystic Fibrosis Trust
Is Referenced By:
\u0027Data Resource Profile: The UK CF Registry\u0027 published in the International Journal of Epidemiology (2018 Feb 1;47(1)9-10e)
Format and Standards
Vocabulary Encoding Schemes:
LOCAL
Conforms To:
LOCAL
Languages:
en
Formats:
csv
Enrichment and Linkage
Qualified Relations:
All our datasets are linked by a common identifier. No external linkages.
Derivations:
Not Applicable
Origin
Name:
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