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National Congenital Anomaly and Rare Disease Registration Service: patient leaflet

• From: Public Health England
• Part of: National Congenital Anomaly and Rare Disease Registration Service
• Published: 1 July 2015

What NCARDRS does, the benefits of registering, and how we look after your information.

Documents

The National Congenital Anomaly and Rare Disease Registration Service: what it is, the benefits and your options

Ref: PHE publications gateway number: 2014821 PDF, 368KB, 2 pages

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Details

GPs and clinicians can use this leaflet when they speak to parents whose baby has a congenital anomaly or rare disease.

GPs and clinicians can contact the regional offices for printed copies of this leaflet.

Document information

Published: 1 July 2015

From: Public Health England

Part of: National Congenital Anomaly and Rare Disease Registration Service