We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
NCARDRS records those people with congenital abnormalities and rare diseases across the whole of England.
Data by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) showing estimates of birth prevalence of congenital anomalies in England.
Information to help healthcare professionals speak with parents, following suspected or confirmed diagnosis of congenital heart disease.
This leaflet can help healthcare professionals speak with people, following suspected or confirmed diagnosis of congenital diaphragmatic hernia (CDH).
The report is based on registration data collected by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) in NDRS (Data Services Directorate).
Advice to give pregnant women on infections that can be transmitted via contact with animals that are or have recently given birth.
This statistical release describes congenital anomalies in babies born or delivered in 2021.
You must tell DVLA if you have congenital heart disease - download the correct form to let them know
Don’t include personal or financial information like your National Insurance number or credit card details.
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).