Study centre number
Item
Site #
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
patient ID
Item
Patient #
integer
C2348585 (UMLS CUI [1])
visit date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Investigator Name
Item
Investigator Name
text
C2826892 (UMLS CUI [1])
Date of informed consent/assent
Item
Date consent form/assent signed:
date
C2985782 (UMLS CUI [1])
C5205794 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
Informed consent time
Item
Time consent form/assent signed:
time
C5206390 (UMLS CUI [1])
C5205794 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
date of birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Duration of gestation
Item
If patient is < 6 months old, number weeks gestation:
integer
C0460089 (UMLS CUI [1])
Corrected age
Item
Corrected gestational age
integer
C3831006 (UMLS CUI [1])
Item
Race
text
C0034510 (UMLS CUI [1])
CL Item
Caucasian (Caucasian)
CL Item
Hispanic (Hispanic)
CL Item
Other, Specify: (Other)
Other race, specify
Item
Other race, specify:
text
C0034510 (UMLS CUI [1,1])
C3845569 (UMLS CUI [1,2])