
Cutting through the Diagnostic Maze for Rare Diseases
Apr 30, 2026 - 00:38:56
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Matching phenotype to genotype at scale could transform how rare diseases are found, understood, and treated. Komodo Health has partnered with GeneDx to build one of the most comprehensive longitudinal rare disease datas...
Using AI and Longitudinal Data to Transform Rare Disease Care is an episode from RARECast by RARECast. Matching phenotype to genotype at scale could transform how rare diseases are found, understood, and treated. Komodo Health has partnered...
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Published May 7, 2026, 00:19:21 long, audio available.
Matching phenotype to genotype at scale could transform how rare diseases are found, understood, and treated. Komodo Health has partnered with GeneDx to build one of the most comprehensive longitudinal rare disease datasets ever assembled. John Wollman, head of revenue strategy at Komodo Health, discusses how Komodo’s longitudinal real‑world data on more than 330 million de-identified U.S. patient journeys, combined with GeneDx’s genomic testing and rich phenotypic information, can shorten diagnostic odysseys, rapidly enable natural history studies, and help stakeholders across the rare disease continuum make smarter and faster decisions for people living with rare diseases.
You can listen to Using AI and Longitudinal Data to Transform Rare Disease Care online on Radio and Podcast. Open the player on this page to stream the available audio.
Using AI and Longitudinal Data to Transform Rare Disease Care is an episode from RARECast by RARECast.
This episode is 00:19:21 long.
This episode was published on May 7, 2026.
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You can listen to Using AI and Longitudinal Data to Transform Rare Disease Care on this page when the episode audio is available from the podcast feed.
Using AI and Longitudinal Data to Transform Rare Disease Care is from RARECast by RARECast.
Published May 7, 2026 and 00:19:21 long