Description
During the informed consent process, the subject is asked if he/she would like the option of receiving his/her HLA- B*5701 results when the results are available. The subject’s response is captured on the informed consent form using yes/no checkboxes. The subject’s response should be transcribed from the informed consent form to the CRF page.
Data type
text
Alias
- UMLS CUI [1,1]
- C1514756
- UMLS CUI [1,2]
- C0679560
- UMLS CUI [1,3]
- C1274040