This data table contains subject IDs and consent group information for subjects with chronic renal insufficiency.

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This data table contains subject IDs and consent group information for subjects with chronic renal insufficiency.
    3. The data table contains mapping of study subject IDs to sample IDs for subjects with chronic renal insufficiency. 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. Also included is the sample use.
    4. The subject phenotype data table includes self-reported medical history (n=9 variables; asthma, arthritis, COPD, MI/prior revascularization, PVD, CHF, stroke, any CVD, and atrial fibrillation/heart arrythmia), family history (n=2 variables; CAD and renal disease), anthropometric measurements (n=5 variables; height, weight, BMI, BSA, and waist), blood pressure and pulse measures (systolic/diastolic, MAP, pulse, ankle brachial indices), CO2 measurement, lipid data (n=5 variables), diabetes screening (n=2 variables), eGFR, serum lab measurements (n=16 variables), CBC measurements (n=2 variables), urine lab measurements (n=3 variables), Becks and MMSE scores, smoking status (n=2 variables), alcohol use, medications (n=3 variables), and medication indicators (n=47 variables).
    5. The sample attributes data table includes sample analyte type (DNA or RNA), body site where samples were collected, is tumor status, and histological type.
pht002916
Descrizione

pht002916

Subject ID
Descrizione

PID

Tipo di dati

string

Alias
UMLS CUI [1,1]
C2348585
Consent group as determined by DAC
Descrizione

consent

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1257890

Similar models

This data table contains subject IDs and consent group information for subjects with chronic renal insufficiency.

  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This data table contains subject IDs and consent group information for subjects with chronic renal insufficiency.
    3. The data table contains mapping of study subject IDs to sample IDs for subjects with chronic renal insufficiency. 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. Also included is the sample use.
    4. The subject phenotype data table includes self-reported medical history (n=9 variables; asthma, arthritis, COPD, MI/prior revascularization, PVD, CHF, stroke, any CVD, and atrial fibrillation/heart arrythmia), family history (n=2 variables; CAD and renal disease), anthropometric measurements (n=5 variables; height, weight, BMI, BSA, and waist), blood pressure and pulse measures (systolic/diastolic, MAP, pulse, ankle brachial indices), CO2 measurement, lipid data (n=5 variables), diabetes screening (n=2 variables), eGFR, serum lab measurements (n=16 variables), CBC measurements (n=2 variables), urine lab measurements (n=3 variables), Becks and MMSE scores, smoking status (n=2 variables), alcohol use, medications (n=3 variables), and medication indicators (n=47 variables).
    5. The sample attributes data table includes sample analyte type (DNA or RNA), body site where samples were collected, is tumor status, and histological type.
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
pht002916
PID
Item
Subject ID
string
C2348585 (UMLS CUI [1,1])
Item
Consent group as determined by DAC
text
C0021430 (UMLS CUI [1,1])
C1257890 (UMLS CUI [1,2])
Code List
Consent group as determined by DAC
CL Item
All Health Conditions (AHC) (1)
CL Item
Research on Disease of Kidney, Heart and Blood Vessels (KHB) (2)