[3P-0654] The 1^st stage of Initiative on Rare and Undiagnosed Diseases (IRUD): statistics and challenges

〇Tadashi Kaname¹, Kumiko Yanagi¹, Manami Iso¹, Nana Kobayashi¹, Yukimi Abe¹, Meiko Takeshita¹, Yoko Kuroki¹, Keiko Hayashi¹, Kouji Okamura², Hiroko Ogata³, Tomoko Kawai³, Kazuhiko Nakabayashi³, Kenichiro Hata³, Kenjiro Kosaki⁴, Kazuhito Sato¹, Yoichi Matsubara⁵, Consortium IRUD-P⁶ (1.Dept of Gen Med, NCCHD, 2.Dept of system Biomed, Sct of Tissue Eng, NCCHD, 3.Dept Mat-Fetal Biol, NCCHD, 4.Centre for Med Gen, KEIO, 5.NCCHD, 6.AMED)

IRUD, NGS, Whole exome analysis, Hereditary disease, Genetic diagnosis