Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
*SAFHS*
Description

Elig.phs001215.v4.p2.1

Data type

boolean

Alias
UMLS CUI [1,1]
C2348560
The SAFHS began in 1991, and included 1,431 individuals in 42 extended families at baseline. Probands were 40 to 60 year old low-income Mexican Americans selected at random without regard to presence or absence of disease, almost exclusively from Mexican American census tracts in San Antonio, Texas. All first, second, and third degree relatives of the proband and of the proband's spouse, aged 16 years or above, were eligible to participate in the study. As part of our ongoing studies, we have recruited new family members from the original families, expanding the cohort to almost 3,000 individuals.
Description

Elig.phs001215.v4.p2.2

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0237401
UMLS CUI [1,3]
C1292711
UMLS CUI [1,4]
C0015341
UMLS CUI [1,5]
C1442488
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0001779
UMLS CUI [2,3]
C1331016
UMLS CUI [2,4]
C3829110
UMLS CUI [2,5]
C0439605
UMLS CUI [2,6]
C0242802
UMLS CUI [2,7]
C1298908
UMLS CUI [2,8]
C0518609
UMLS CUI [2,9]
C3854307
UMLS CUI [2,10]
C0332197
UMLS CUI [2,11]
C0012634
UMLS CUI [3,1]
C1517194
UMLS CUI [3,2]
C1519210
UMLS CUI [3,3]
C3639750
UMLS CUI [3,4]
C1948021
UMLS CUI [3,5]
C0162409
UMLS CUI [3,6]
C0001779
UMLS CUI [3,7]
C0013893
UMLS CUI [4,1]
C0242800
UMLS CUI [4,2]
C0205314
UMLS CUI [4,3]
C0086282
UMLS CUI [4,4]
C0205313
UMLS CUI [4,5]
C0015576
*WGS efforts*
Description

Elig.phs001215.v4.p2.3

Data type

boolean

Alias
UMLS CUI [1,1]
C4483680
The first T2D-GENES sequencing effort chose the twenty largest pedigrees from SAFHS, constituting approximately 600 individuals. Sequencing in the R01HL113322 "Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk" project selected the next largest pedigrees and participants most informative for imputation, a total of 931 individuals. Finally, sequencing of the remaining SAFHS participants (1199 individuals) was supported by the TOPMed program.
Description

Elig.phs001215.v4.p2.4

Data type

boolean

Alias
UMLS CUI [1,1]
C0205435
UMLS CUI [1,2]
C3640076
UMLS CUI [1,3]
C3715212
UMLS CUI [1,4]
C0443228
UMLS CUI [1,5]
C0030761
UMLS CUI [2,1]
C0242802
UMLS CUI [2,2]
C0205117
UMLS CUI [2,3]
C0443228
UMLS CUI [2,4]
C0030761
UMLS CUI [2,5]
C0205393
UMLS CUI [2,6]
C2986490
UMLS CUI [2,7]
C2699638
UMLS CUI [3,1]
C3640076
UMLS CUI [3,2]
C1527428
UMLS CUI [3,3]
C0679646
UMLS CUI [3,4]
C0242356
UMLS CUI [3,5]
C3484370

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.phs001215.v4.p2.1
Item
*SAFHS*
boolean
C2348560 (UMLS CUI [1,1])
Elig.phs001215.v4.p2.2
Item
The SAFHS began in 1991, and included 1,431 individuals in 42 extended families at baseline. Probands were 40 to 60 year old low-income Mexican Americans selected at random without regard to presence or absence of disease, almost exclusively from Mexican American census tracts in San Antonio, Texas. All first, second, and third degree relatives of the proband and of the proband's spouse, aged 16 years or above, were eligible to participate in the study. As part of our ongoing studies, we have recruited new family members from the original families, expanding the cohort to almost 3,000 individuals.
boolean
C1512693 (UMLS CUI [1,1])
C0237401 (UMLS CUI [1,2])
C1292711 (UMLS CUI [1,3])
C0015341 (UMLS CUI [1,4])
C1442488 (UMLS CUI [1,5])
C0681850 (UMLS CUI [2,1])
C0001779 (UMLS CUI [2,2])
C1331016 (UMLS CUI [2,3])
C3829110 (UMLS CUI [2,4])
C0439605 (UMLS CUI [2,5])
C0242802 (UMLS CUI [2,6])
C1298908 (UMLS CUI [2,7])
C0518609 (UMLS CUI [2,8])
C3854307 (UMLS CUI [2,9])
C0332197 (UMLS CUI [2,10])
C0012634 (UMLS CUI [2,11])
C1517194 (UMLS CUI [3,1])
C1519210 (UMLS CUI [3,2])
C3639750 (UMLS CUI [3,3])
C1948021 (UMLS CUI [3,4])
C0162409 (UMLS CUI [3,5])
C0001779 (UMLS CUI [3,6])
C0013893 (UMLS CUI [3,7])
C0242800 (UMLS CUI [4,1])
C0205314 (UMLS CUI [4,2])
C0086282 (UMLS CUI [4,3])
C0205313 (UMLS CUI [4,4])
C0015576 (UMLS CUI [4,5])
Elig.phs001215.v4.p2.3
Item
*WGS efforts*
boolean
C4483680 (UMLS CUI [1,1])
Elig.phs001215.v4.p2.4
Item
The first T2D-GENES sequencing effort chose the twenty largest pedigrees from SAFHS, constituting approximately 600 individuals. Sequencing in the R01HL113322 "Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk" project selected the next largest pedigrees and participants most informative for imputation, a total of 931 individuals. Finally, sequencing of the remaining SAFHS participants (1199 individuals) was supported by the TOPMed program.
boolean
C0205435 (UMLS CUI [1,1])
C3640076 (UMLS CUI [1,2])
C3715212 (UMLS CUI [1,3])
C0443228 (UMLS CUI [1,4])
C0030761 (UMLS CUI [1,5])
C0242802 (UMLS CUI [2,1])
C0205117 (UMLS CUI [2,2])
C0443228 (UMLS CUI [2,3])
C0030761 (UMLS CUI [2,4])
C0205393 (UMLS CUI [2,5])
C2986490 (UMLS CUI [2,6])
C2699638 (UMLS CUI [2,7])
C3640076 (UMLS CUI [3,1])
C1527428 (UMLS CUI [3,2])
C0679646 (UMLS CUI [3,3])
C0242356 (UMLS CUI [3,4])
C3484370 (UMLS CUI [3,5])