Prohibited use of registry information.

S.C. Code Ann. § 44-33-340
in effect
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The information maintained in the Sickle Cell Disease Voluntary Patient Registry may not be released to or used by an entity responsible for the licensure, regulation, or discipline of physicians or other health care practitioners for any purpose.
Source: Open US Law by Vaquill AI (CC BY 4.0)URL: https://www.scstatehouse.gov/code/t44c033.phpFetched: 10/17/2026

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