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Ehlers-Danlos syndrome, type 3

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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

    Total # Biosets: 614

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Thought leaders and organizations working on research involving Benign hypermobility syndrome.

  • R Grahame
  • Lars Remvig
  • Rodney Grahame
  • Nilay Sahin
  • Ender Berker
  • Canadian Memorial Chiropractic College
  • Norwegian School of Sport Sciences
  • Selcuk University
  • City Hospital
  • Copenhagen University
  • Queen Mary University of London
  • University of São Paulo

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