Item
Has informed consent been obtained for PGx research?
text
C0021430 (UMLS CUI [1,1])
C0031325 (UMLS CUI [1,2])
C0035168 (UMLS CUI [1,3])
Code List
Has informed consent been obtained for PGx research?
If Yes, record the date informed consent obtained for PGx research
Item
If Yes, record the date informed consent obtained for PGx research
date
C0011008 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Item
Has a blood sample been collected for PGx research?
text
C0200345 (UMLS CUI [1,1])
C0031325 (UMLS CUI [1,2])
C0035168 (UMLS CUI [1,3])
Code List
Has a blood sample been collected for PGx research?
If Yes, record the date sample taken
Item
If Yes, record the date sample taken
date
C0011008 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
Item
Has subject withdrawn consent for PGx research?
text
C2349954 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Code List
Has subject withdrawn consent for PGx research?
If Yes, record the date informed consent withdrawn for PGx research
Item
If Yes, record the date informed consent withdrawn for PGx research
date
C0011008 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
Item
Has a request been made for blood sample destruction?
text
C0686900 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
Code List
Has a request been made for blood sample destruction?
Item
If Yes, choose one reason:
text
C0392360 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
Code List
If Yes, choose one reason:
CL Item
Subject withdrew consent for PGx (3)
CL Item
Screen failure (2)
If other, specify:
Item
If other, specify:
text
C2348235 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,4])