Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
The study recruited Caucasian participants primarily from three-generational pedigrees from two NHLBI Family Heart Study (FHS) field centers (Minneapolis, MN and Salt Lake City, UT). Only families with at least two siblings were recruited and only participants who did not take lipid-lowering agents (pharmaceuticals or nutraceuticals) for at least 4 weeks prior to the initial visit were included.
Description

Elig.phs000741.v2.p1.1

Data type

boolean

Alias
UMLS CUI [1,1]
C1698493
UMLS CUI [1,2]
C0043157
UMLS CUI [1,3]
C0205449
UMLS CUI [1,4]
C0079411
UMLS CUI [1,5]
C3669174
UMLS CUI [2,1]
C0242800
UMLS CUI [2,2]
C0015576
UMLS CUI [2,3]
C0205448
UMLS CUI [2,4]
C0037047
UMLS CUI [3,1]
C1298908
UMLS CUI [3,2]
C0585943
UMLS CUI [3,3]
C1442465
UMLS CUI [3,4]
C0332152
UMLS CUI [3,5]
C0545082

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000741.v2.p1.1
Item
The study recruited Caucasian participants primarily from three-generational pedigrees from two NHLBI Family Heart Study (FHS) field centers (Minneapolis, MN and Salt Lake City, UT). Only families with at least two siblings were recruited and only participants who did not take lipid-lowering agents (pharmaceuticals or nutraceuticals) for at least 4 weeks prior to the initial visit were included.
boolean
C1698493 (UMLS CUI [1,1])
C0043157 (UMLS CUI [1,2])
C0205449 (UMLS CUI [1,3])
C0079411 (UMLS CUI [1,4])
C3669174 (UMLS CUI [1,5])
C0242800 (UMLS CUI [2,1])
C0015576 (UMLS CUI [2,2])
C0205448 (UMLS CUI [2,3])
C0037047 (UMLS CUI [2,4])
C1298908 (UMLS CUI [3,1])
C0585943 (UMLS CUI [3,2])
C1442465 (UMLS CUI [3,3])
C0332152 (UMLS CUI [3,4])
C0545082 (UMLS CUI [3,5])