OMIM ID

Use this field to specify the variable containing the OMIM ID.

The OMIM ID is a unique identifier assigned to a genetic disorder in the Online Mendelian Inheritance in Man. OMIM is a directory of human genes and genetic disorders, with links to literature references, sequence records, maps, and related databases.

This variable is used to make the web search link to the OMIM database.

To Specify a Variable Containing the OMIM ID:

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Specify an {link}{Emphasis}Input SAS Data Set.

The Available Variables field is populated with variables from the specified data set.

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Highlight a variable from the Available Variables field.

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Click to add the selected variable to the OMIM ID field.