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Rare Disease Registries (e.g., Li-Fraumeni Syndrome International Registry, Bloom's Syndrome Registry)

A)Used to input patient registration information, which results in creation of an automated master patient index database that allows for the storage and retrieval of the information.
B)Collect clinical and genetic data -Provide referrals to genetic counseling and other services -Conduct ongoing research

1 Answer

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Final answer:

The Online Mendelian Inheritance in Man (OMIM) database provides comprehensive information about genes for genetic diseases and their inheritance. It also offers suggestions for treatments, supporting and guiding research for rare genetic conditions like progeria.

Step-by-step explanation:

The Online Mendelian Inheritance in Man (OMIM) database can support and guide research for rare genetic conditions, like progeria, by providing all the information about genes for genetic diseases, their inheritance, and their expression. The database also provides suggestions for some treatments. By accessing this database, researchers can identify and study disease genes more effectively, which can help in the development of potential treatments and prevention strategies.

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