NCARDRS congenital anomaly statistics: annual data
Data by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) showing estimates of birth prevalence of congenital anomalies in England.
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The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) reports present data collected since 2014.
These reports give estimates of the national prevalence of congenital anomalies using data from the NCARDRS regions relevant for the reporting period.
The reports include data relating to a wide range of congenital anomalies including structural, chromosomal and genetic anomalies. The 2015 report also includes a chapter specifically on Down’s syndrome, Edwards’ syndrome and Patau’s syndrome, presenting data on all cases in England up to 2016.
Last updated 29 September 2021 + show all updates
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Added main report, summary, technical details and data tables for 2019.
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Added link to anonymous survey about the congenital anomaly statistics report.
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Added 2018 updates: summary report, statistics, technical details and tables.
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Added executive summary of the NCARDRS statistics 2017 report.
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Added 2017 NCARDRS statistics reports and spreadsheet.
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Added 2016 'summary report', 'Congenital anomaly statistics', 'tables', and 'glossary and technical details'.
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First published.