PRaGeD and structured genomic data
The paediatric rare-disease mission is moving toward unified clinical and genomic records across centres.
The Mission Program on Pediatric Rare Genetic Disorders (PRaGeD) is a pan-India effort to diagnose undiagnosed childhood genetic disease and to discover new genes. Centres in the network are adopting shared, structured clinical and genomic data systems so that diagnoses, counselling, and research can travel with the family rather than sit in a single laboratory.
Programme films in several Indian languages are collected on the Videos page.