[2P-1103] Initiative on rare and undiagnosed diseases

〇Tadashi Kaname¹, Kumiko Yanagi¹, Mari Minatogawa¹, Manami Iso¹, Kana Hosoki¹, Yoko Kuroki¹, Koji Okamura², Hiroko Ogata³, Kazuhiko Nakabayashi³, Tomoko Kawai³, Kenichiro Hata³, Kazuhito Satou¹, Kenjiro Kosaki⁴, Yoichi Matsubara⁵ (1.Dept Gen Med, NCCHD, 2.Divis Tissue Engnr, NCCHD, 3.Dept Mat-Fetal Biol, NCCHD, 4.Ctr Med Genet, Keio Univ Sch Med, 5.Natl Inst Child Health Develop, NCCHD)

IRUD、Whole exome analysis、Genetic diseases、Drug discovery、Next-generation sequencer