Research and analysis

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.

• From: Public Health England
• Published: 20 July 2017
• Last updated: 29 September 2021
  Show all updates

  1. 29 September 2021

     Added main report, summary, technical details and data tables for 2019.

  2. 16 September 2021

     Added link to anonymous survey about the congenital anomaly statistics report.

  3. 12 August 2020

     Added 2018 updates: summary report, statistics, technical details and tables.

  4. 9 August 2019

     Added executive summary of the NCARDRS statistics 2017 report.

  5. 2 August 2019

     Added 2017 NCARDRS statistics reports and spreadsheet.

  6. 19 October 2018

     Added 2016 'summary report', 'Congenital anomaly statistics', 'tables', and 'glossary and technical details'.

  7. 20 July 2017

     First published.

Documents

NCARDRS statistics 2019: summary report

Ref: PHE publications gateway number: GOV-9201

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NCARDRS congenital anomaly statistics 2019

Ref: PHE publications gateway number: GOV-9201

PDF, 1.82 MB, 41 pages

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NCARDRS congenital anomaly statistics 2019: technical details

Ref: PHE publications gateway number: GOV-9201

PDF, 787 KB, 31 pages

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NCARDRS congenital anomaly statistics 2019: tables

Ref: PHE publications gateway number: GOV-9201

MS Excel Spreadsheet, 56.3 KB

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NCARDRS statistics 2018: summary report

Ref: PHE publications gateway number: GW-1445

HTML

NCARDRS congenital anomaly statistics 2018

Ref: PHE publications gateway number: GW-1445

PDF, 1.7 MB, 43 pages

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NCARDRS congenital anomaly statistics 2018: technical details

Ref: PHE publications gateway number: GW-1445

PDF, 812 KB, 22 pages

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NCARDRS congenital anomaly statistics 2018: tables

Ref: PHE publications gateway number: GW-1445

ODS, 34.7 KB

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NCARDRS statistics 2017: summary report

Ref: PHE publications gateway number: GW-473

HTML

NCARDRS congenital anomaly statistics 2017

Ref: PHE publications gateway number GW-473

PDF, 1.34 MB, 36 pages

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NCARDRS congenital anomaly statistics 2017: technical details

Ref: PHE publications gateway number GW-473

PDF, 741 KB, 17 pages

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NCARDRS congenital anomaly statistics 2017: tables

Ref: PHE publications gateway number GW-473

ODS, 38.4 KB

This file is in an OpenDocument format

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NCARDRS statistics 2016: summary report

Ref: PHE publications gateway number 2018527

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NCARDRS congenital anomaly statistics 2016

Ref: PHE publications gateway number 2018527

PDF, 939 KB, 29 pages

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NCARDRS congenital anomaly statistics 2016: tables

Ref: PHE publications gateway number 2018527

PDF, 446 KB, 13 pages

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NCARDRS congenital anomaly statistics 2016: glossary and technical details

Ref: PHE publications gateway number 2018527

PDF, 590 KB, 17 pages

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NCARDRS congenital anomaly statistics 2015

Ref: PHE publications gateway number 2017200

PDF, 1.2 MB, 48 pages

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Details

If you have read the congenital anomaly statistics report, we would greatly appreciate your feedback. It will help us understand how the report is being used and how to improve it. Please fill in this anonymous survey.

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.