The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS), part of the National Disease Registration Service in NHS England, is a comprehensive registration service that collects, and quality assures data on congenital anomalies and rare diseases in England.
Series / Collection
NCARDRS Congenital Anomaly Statistics: Annual Data
Official statistics- Frequency:
- Yearly
- Geographic Coverage:
- England
- Geographical Granularity:
Summary
Past publications
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In April 2025, NCARDRS turned 10 years old, and with this report, provides national data for the 5th consecutive year. In a decade, congenital condition...
23 October 2025
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This publication contains information on congenital anomalies detected in babies delivered in England between 1 January and 31 December 2021.
28 March 2024
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This publication contains information on congenital anomalies in babies delivered in England in 2020. It includes this report showing key findings, spreadsheet...
1 December 2022