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Nationwide comprehensive epidemiological study of rare diseases in Japan using a health insurance claims database.

Kota NinomiyaMasahiro Okura
Published in: Orphanet journal of rare diseases (2022)
Our research revealed the basic epidemiology and natural history of Japanese patients with some rare diseases using a health insurance claims database. The results imply that the coverage of the present Nanbyo systems is inadequate for rare diseases. Therefore, fundamental reform might be needed to reduce unfairness between rare diseases. Most diseases in Japan follow a tendency of natural history similar to those reported in Orphanet. However, some are detected later, partly because fewer clinical genetic tests are available in Japan than in the West. Finally, we hope that our data and analysis accelerate drug discovery for rare diseases in Japan.
Keyphrases
  • health insurance
  • affordable care act
  • gene expression
  • dna methylation
  • artificial intelligence