Answer First
Primary Text
Registration of Persons with Rare Disease. All healthcare practitioners and health institutions shall be required to report to the Rare Disease Registry diagnosed cases of rare disease and provide reports on the status of patients: Provided, That such reports shall be subject to guidelines issued by the NIH to protect the privacy of patients with rare disease.
ARTICLE IV
PERSONS WITH RARE DISEASE AS PERSONS WITH DISABILITIES (PWDs)
Use With Care
Definitions and exceptions often appear before or after this text.
Court decisions may interpret, limit, or apply this provision.
Confirm amendment, repeal, effectivity, and official publication.