Which social identifying information is required in the Parkinson's Disease registry report?

The requirement for including the patient's social security number in the Parkinson's Disease registry report stems from the need for accurate identification and tracking of individuals diagnosed with the disease. The social security number serves as a unique identifier that helps to ensure that information is linked to the correct individual, which is especially important in a registry that may involve healthcare providers and state agencies.

Using social security numbers in this context allows for more efficient data management and helps avoid duplication in records. It also aids in maintaining the integrity of the data collected, as each patient can be distinctly identified among potentially large populations. This is particularly pertinent for health registries where personal information confidentiality and tracking for research or healthcare purposes are crucial.

In contrast, the other options—health insurance policy number, birth certificate number, and driver's license number—do not provide the same level of unique identification or may lack the designated use in registries like the one for Parkinson's Disease. While they may be useful in healthcare settings, they are not standard identifiers required for registry reporting purposes.