Elig.phs001073.v2.p1.1
Item
Criteria for the PROVIDE Study are as follows: Inclusion Criteria <br>
boolean
C1512693 (UMLS CUI [1,1])
Elig.phs001073.v2.p1.2
Item
Mother willing to sign informed consent form.
boolean
C0026591 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
Elig.phs001073.v2.p1.3
Item
Healthy infant aged 0 to 7 days old.
boolean
C3898900 (UMLS CUI [1,1])
C0021270 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
Elig.phs001073.v2.p1.4
Item
No obvious congenital abnormalities or birth defects.
boolean
C1298908 (UMLS CUI [1,1])
C0000768 (UMLS CUI [1,2])
Elig.phs001073.v2.p1.5
Item
No abnormal (frequency and consistency) stools since birth.
boolean
C1298908 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
C0015733 (UMLS CUI [1,3])
C1711239 (UMLS CUI [1,4])
C0005615 (UMLS CUI [1,5])
Elig.phs001073.v2.p1.6
Item
Stable household with no plans to leave the area for the next one year. <br> Exclusion Criteria <br>
boolean
C0205360 (UMLS CUI [1,1])
C0020052 (UMLS CUI [1,2])
C1298908 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
C2699029 (UMLS CUI [1,5])
C0680251 (UMLS CUI [2,1])
Elig.phs001073.v2.p1.7
Item
Parents are not willing to have child vaccinated at the field clinic.
boolean
C0030551 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0008059 (UMLS CUI [1,3])
C0042196 (UMLS CUI [1,4])
C0442592 (UMLS CUI [1,5])
Elig.phs001073.v2.p1.8
Item
Parents are not willing to have child's blood drawn.
boolean
C0030551 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0008059 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
Elig.phs001073.v2.p1.9
Item
Parents are planning to enroll child into another clinical study during the time period of this trial.
boolean
C1301732 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0347984 (UMLS CUI [1,5])
C2347804 (UMLS CUI [1,6])
Elig.phs001073.v2.p1.10
Item
Mother not willing to have blood drawn and breast milk extracted.
boolean
C0026591 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,3])
C0026131 (UMLS CUI [1,4])
C0185115 (UMLS CUI [1,5])
Elig.phs001073.v2.p1.11
Item
Parents not willing to have field research assistant in home two times per week.
boolean
C0030551 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0035173 (UMLS CUI [1,3])
C0020043 (UMLS CUI [1,4])
C0205448 (UMLS CUI [1,5])
C0456698 (UMLS CUI [1,6])
Elig.phs001073.v2.p1.12
Item
History of seizures or other apparent neurologic disorders.
boolean
C0262926 (UMLS CUI [1,1])
C0036572 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0027765 (UMLS CUI [1,4])
Elig.phs001073.v2.p1.13
Item
Infant received any vaccines before start of study, except Bacillus Calmette-Guerin (BCG).
boolean
C0021270 (UMLS CUI [1,1])
C2368628 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C2347804 (UMLS CUI [1,4])
C1705847 (UMLS CUI [1,5])
C0004886 (UMLS CUI [1,6])
Elig.phs001073.v2.p1.14
Item
Infant has any sibling currently or previously enrolled in this study, including a twin.
boolean
C0021270 (UMLS CUI [1,1])
C1552551 (UMLS CUI [1,2])
C0037047 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C1516879 (UMLS CUI [1,5])
C0008976 (UMLS CUI [1,6])
Elig.phs001073.v2.p1.15
Item
Criteria for the Epigenetic Analysis of Malnutrition study include meeting the inclusion criteria for the PROVIDE study and either being stunted (a height for age Z score of 2 standard deviations under the WHO's mean) or of normal height for age. These criteria were chosen so that meaningful differences in H3K4me3 expression could be detected between malnourished and well-nourished participants.
boolean
C1512693 (UMLS CUI [1,1])
C4329794 (UMLS CUI [1,2])
C0936012 (UMLS CUI [1,3])
C0162429 (UMLS CUI [1,4])
C0008972 (UMLS CUI [1,5])
C1516637 (UMLS CUI [1,6])
C1550543 (UMLS CUI [1,7])
C4230744 (UMLS CUI [1,8])
C0587053 (UMLS CUI [1,9])
C1511790 (UMLS CUI [2,1])
C1705242 (UMLS CUI [2,2])
C3846158 (UMLS CUI [2,3])
C0017262 (UMLS CUI [2,4])
C0162429 (UMLS CUI [2,5])
C0517226 (UMLS CUI [2,6])
C0679646 (UMLS CUI [2,7])