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Revolutionary coding standard to transform rare disease diagnosis | UNC-Chapel Hill

When Ezra Barnes was 4 months old, he was unable to sit without support and later failed to reach other developmental milestones, prompting his worried parents to consult several medical experts. “The doctors all came back to us to say that they didn’t have a diagnosis,” said his mother, Coryssa Barnes, of Henderson, North Carolina. “We had a mix of anxiety and nerves because you don’t want anything to be wrong with your kid.” After a year, Ezra…
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The University of North Carolina at Chapel Hill… broke the news in on Monday, March 16, 2026.
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