Eligibility Criteria

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status. All subjects are controls for studying continuous traits from echocardiography exams.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, sex of subjects, and monozygotic twin IDs.
    4. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
    5. This subject phenotypes data table includes age, sex, race, education, field center and lab ID, medical history (n=13 variables; menopause, pregnancy, preeclampsia, hormone medication, heart attack, heart bypass, and stroke), hypertension status (n=2 variables), diabetes status, anthropometric measures (n=15 variables; waist, hip, triceps, subscapularis, elbow, weight, height, BMI, percent body fat), blood pressure and pulse (n=33 variables; systolic, diastolic, sitting, standing, mean arterial pressure), echocardiographic measurements (n=12 variables), blood and urine measurements (n=34 variables), medications (n=12 variables), alcohol use (n=11 variables), and smoking status (n=4 variables).
    6. This sample attributes table includes body site where sample was collected, analyte type, tumor status, sequencing center, funding source, TOPMed phase, project, and study name.
Inclusion and exclusion criteria
Descrizione

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
HyperGEN recruited 470 multiply-affected population-based hypertensive AA sibships (N=1224 siblings) from 1996-1999. HyperGEN probands were ascertained by early onset hypertension (i.e., before 60 years); to participate, they had to have at least one hypertensive sibling who was also willing to participate. Hypertension was defined according to antihypertensive treatment or BP (systolic BP ≥140 or diastolic BP ≥90 measured on at least at two time points); Type 1 diabetes and renal failure were exclusion criteria. The HyperGEN study extended recruitment to include all offspring (n=546) of the proband and his/her siblings during the second 5-year funding period. HyperGEN also recruited participants randomly selected from the source cohorts where the families were ascertained to represent population allele frequencies; 414 African American participants were recruited randomly. In total, ~2,200 African-American participants were examined and gave permission for DNA testing and sharing from sites in Birmingham, AL and Winston-Salem, NC. Of those ~2000 have data recorded from an echocardiography exam and were included in the TOPMed study of LV hypertrophy and related traits.
Descrizione

Elig.phs001293.v3.p1.1

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0242800
UMLS CUI [1,2]
C0037047
UMLS CUI [1,3]
C1279919
UMLS CUI [1,4]
C0332162
UMLS CUI [1,5]
C0020538
UMLS CUI [2,1]
C1512693
UMLS CUI [2,2]
C0037047
UMLS CUI [2,3]
C0020538
UMLS CUI [2,4]
C0600109
UMLS CUI [2,5]
C0679823
UMLS CUI [3,1]
C1704788
UMLS CUI [3,2]
C0020538
UMLS CUI [3,3]
C0003364
UMLS CUI [3,4]
C0005823
UMLS CUI [4,1]
C0680251
UMLS CUI [4,2]
C0011854
UMLS CUI [4,3]
C0035078
UMLS CUI [5,1]
C0242800
UMLS CUI [5,2]
C1512693
UMLS CUI [5,3]
C0680063
UMLS CUI [6,1]
C0242800
UMLS CUI [6,2]
C0449416
UMLS CUI [6,3]
C0599755
UMLS CUI [6,4]
C1882932
UMLS CUI [6,5]
C4722262
UMLS CUI [7,1]
C0242800
UMLS CUI [7,2]
C0085756
UMLS CUI [7,3]
C0150105
UMLS CUI [8,1]
C0085756
UMLS CUI [8,2]
C0031809
UMLS CUI [8,3]
C0521104
UMLS CUI [8,4]
C0200898
UMLS CUI [9,1]
C1265611
UMLS CUI [9,2]
C3669169
UMLS CUI [9,3]
C0013516
UMLS CUI [9,4]
C1512693
UMLS CUI [9,5]
C0008976
UMLS CUI [9,6]
C0149721
UMLS CUI [9,7]
C0599883

Similar models

Eligibility Criteria

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status. All subjects are controls for studying continuous traits from echocardiography exams.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, sex of subjects, and monozygotic twin IDs.
    4. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
    5. This subject phenotypes data table includes age, sex, race, education, field center and lab ID, medical history (n=13 variables; menopause, pregnancy, preeclampsia, hormone medication, heart attack, heart bypass, and stroke), hypertension status (n=2 variables), diabetes status, anthropometric measures (n=15 variables; waist, hip, triceps, subscapularis, elbow, weight, height, BMI, percent body fat), blood pressure and pulse (n=33 variables; systolic, diastolic, sitting, standing, mean arterial pressure), echocardiographic measurements (n=12 variables), blood and urine measurements (n=34 variables), medications (n=12 variables), alcohol use (n=11 variables), and smoking status (n=4 variables).
    6. This sample attributes table includes body site where sample was collected, analyte type, tumor status, sequencing center, funding source, TOPMed phase, project, and study name.
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs001293.v3.p1.1
Item
HyperGEN recruited 470 multiply-affected population-based hypertensive AA sibships (N=1224 siblings) from 1996-1999. HyperGEN probands were ascertained by early onset hypertension (i.e., before 60 years); to participate, they had to have at least one hypertensive sibling who was also willing to participate. Hypertension was defined according to antihypertensive treatment or BP (systolic BP ≥140 or diastolic BP ≥90 measured on at least at two time points); Type 1 diabetes and renal failure were exclusion criteria. The HyperGEN study extended recruitment to include all offspring (n=546) of the proband and his/her siblings during the second 5-year funding period. HyperGEN also recruited participants randomly selected from the source cohorts where the families were ascertained to represent population allele frequencies; 414 African American participants were recruited randomly. In total, ~2,200 African-American participants were examined and gave permission for DNA testing and sharing from sites in Birmingham, AL and Winston-Salem, NC. Of those ~2000 have data recorded from an echocardiography exam and were included in the TOPMed study of LV hypertrophy and related traits.
boolean
C0242800 (UMLS CUI [1,1])
C0037047 (UMLS CUI [1,2])
C1279919 (UMLS CUI [1,3])
C0332162 (UMLS CUI [1,4])
C0020538 (UMLS CUI [1,5])
C1512693 (UMLS CUI [2,1])
C0037047 (UMLS CUI [2,2])
C0020538 (UMLS CUI [2,3])
C0600109 (UMLS CUI [2,4])
C0679823 (UMLS CUI [2,5])
C1704788 (UMLS CUI [3,1])
C0020538 (UMLS CUI [3,2])
C0003364 (UMLS CUI [3,3])
C0005823 (UMLS CUI [3,4])
C0680251 (UMLS CUI [4,1])
C0011854 (UMLS CUI [4,2])
C0035078 (UMLS CUI [4,3])
C0242800 (UMLS CUI [5,1])
C1512693 (UMLS CUI [5,2])
C0680063 (UMLS CUI [5,3])
C0242800 (UMLS CUI [6,1])
C0449416 (UMLS CUI [6,2])
C0599755 (UMLS CUI [6,3])
C1882932 (UMLS CUI [6,4])
C4722262 (UMLS CUI [6,5])
C0242800 (UMLS CUI [7,1])
C0085756 (UMLS CUI [7,2])
C0150105 (UMLS CUI [7,3])
C0085756 (UMLS CUI [8,1])
C0031809 (UMLS CUI [8,2])
C0521104 (UMLS CUI [8,3])
C0200898 (UMLS CUI [8,4])
C1265611 (UMLS CUI [9,1])
C3669169 (UMLS CUI [9,2])
C0013516 (UMLS CUI [9,3])
C1512693 (UMLS CUI [9,4])
C0008976 (UMLS CUI [9,5])
C0149721 (UMLS CUI [9,6])
C0599883 (UMLS CUI [9,7])