*Inclusion Criteria*
Item
*Inclusion Criteria*
boolean
C1512693 (UMLS CUI [1,1])
HIV-infected patients
Item
HIV-infected patients
boolean
C0019693 (UMLS CUI [1,1])
ART naÏve patients who Initiated EFV-containing ART regimens during clinical care at Vanderbilt Comprehensive Care Center in Nashville, TN from 1998 to 2012.
Item
ART naÏve patients who Initiated EFV-containing ART regimens during clinical care at Vanderbilt Comprehensive Care Center in Nashville, TN from 1998 to 2012.
boolean
C1963724 (UMLS CUI [1,1])
C0332256 (UMLS CUI [1,2])
C0674428 (UMLS CUI [1,3])
C1963724 (UMLS CUI [1,4])
C1947933 (UMLS CUI [1,5])
C1552443 (UMLS CUI [1,6])
Patients who had at least one follow-up visit after ART initiation visit.
Item
Patients who had at least one follow-up visit after ART initiation visit.
boolean
C0589121 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
Patients who provided written informed consent for genetic testing through the CFAR Data and Specimen Repository.
Item
Patients who provided written informed consent for genetic testing through the CFAR Data and Specimen Repository.
boolean
C0021430 (UMLS CUI [1,1])
C1320549 (UMLS CUI [1,2])
C1541218 (UMLS CUI [1,3])
C3847505 (UMLS CUI [1,4])
Patients who had genotype data in *CYP2B6*, *CYP2A6* and whole genome exome data.
Item
Patients who had genotype data in *CYP2B6*, *CYP2A6* and whole genome exome data.
boolean
C0017431 (UMLS CUI [1,1])
C1382176 (UMLS CUI [1,2])
C1413868 (UMLS CUI [1,3])
C5446360 (UMLS CUI [1,4])
*Exclusion Criteria*
Item
*Exclusion Criteria*
boolean
C0680251 (UMLS CUI [1,1])
Initiated the EFV-containing regimen during participation in an ACTG clinical trial.
Item
Initiated the EFV-containing regimen during participation in an ACTG clinical trial.
boolean
C0674428 (UMLS CUI [1,1])
C1276413 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])