NCARDRS Congenital Anomaly Statistics Report, 2020
The report is based on registration data collected by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) in NDRS (Data Services Directorate).
The report is based on registration data collected by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) in NDRS (Data Services Directorate).
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).