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    • Disorder Definitions
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    • Glossary
    • Resources
  • Get Involved
    • Studies
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    • Disorder Definitions
    • Publications
    • Collaborating With STAIR
  • News & Events
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Resources

  Learn More   >   Resources
  • Smith-Lemli-Opitz Syndrome
    • Smith-Lemli-Opitz/RSH Foundation
  • Sjögren-Larsson Syndrome
    • United Leukodystrophy Foundation
    • Foundation for Ichthyosis & Related Skin Types
  • Mevalonate Kinase Deficiency/HIDS
    • Autoinflammatory Alliance
  • Congenital Disorders of Glycosylation
    • RareConnect
  • Sitosterolemia
    • Sitosterolemia Foundation - Coming Soon
  • Cerebrotendinous Xanthomatosis
    • United Leukodystrophy Foundation
  • Peroxisomal Biogenesis Disorders
    • Global Foundation for Peroxisomal Disorders

  • NIH Undiagnosed Disease Program
  • National Organization for Rare Disorders (NORD)
  • Office for Human Research Protections
  • Genetics Home Reference
  • Genetic Alliance
  • Clinicaltrials.gov
  • Office of Rare Diseases Research, NCATS
Resources

 

 

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The STAIR (U54HD061939) was a part of the Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research (ORDR), NCATS. This consortium was funded through a collaboration between the NCATS and the NICHD.