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Hypouricemia

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Individual Studies
  • OMIM - Congenital disorder

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data

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Thought leaders and organizations working on research involving hypouricemia.

  • Hitoshi Endou
  • Kimiyoshi Ichida
  • Tatsuo Hosoya
  • Makoto Hosoyamada
  • Hirotaka Matsuo
  • Niigata City General Hospital
  • Akita University School of Medicine
  • Kyorin University School of Medicine
  • Assaf Harofeh Medical Center
  • Seoul National University Children's Hospital

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