Engels

Subject ID, subject source, source subject ID, and consent group of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.

7 Formulieren  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, subject source, source subject ID, and consent group of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    3. Subject ID, sex, monozygous twins, family ID, mother ID, father ID, and sex of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    4. Subject ID, sample ID, and sample use variable obtained from participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    5. Subject ID, array, African Principal Component, East Asian Principal Component, European Principal Component, and Latin Principal Component of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    6. Subject ID, sex, race, affection status, age, BMI, Gleason Summary Score, histologic grading and differentiation, and SEER general summary stage of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    7. Sample ID, package, analyte type, body site where sample was collected, tumor status of sample, and Reagent Kit of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
pht007157
Beschrijving

pht007157

Alias
UMLS CUI [1,1]
C3846158
De-identified subject ID
Beschrijving

SUBJECT_ID

Datatype

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348585
Consent group
Beschrijving

CONSENT

Datatype

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0441833
Subject source
Beschrijving

SUBJECT_SOURCE

Datatype

text

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0449416
Source subject ID
Beschrijving

SOURCE_SUBJECT_ID

Datatype

text

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C0449416
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Similar models

Subject ID, subject source, source subject ID, and consent group of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.

7 Formulieren
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, subject source, source subject ID, and consent group of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    3. Subject ID, sex, monozygous twins, family ID, mother ID, father ID, and sex of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    4. Subject ID, sample ID, and sample use variable obtained from participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    5. Subject ID, array, African Principal Component, East Asian Principal Component, European Principal Component, and Latin Principal Component of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    6. Subject ID, sex, race, affection status, age, BMI, Gleason Summary Score, histologic grading and differentiation, and SEER general summary stage of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
    7. Sample ID, package, analyte type, body site where sample was collected, tumor status of sample, and Reagent Kit of participants with or without prostate cancer and involved in the "ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer" project.
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
pht007157
C3846158 (UMLS CUI [1,1])
SUBJECT_ID
Item
De-identified subject ID
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Item
Consent group
text
C0021430 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
CONSENT
Code List
Consent group
CL Item
Subjects did not participate in the study, did not complete a consent document and are included only for the pedigree structure and/or genotype controls, such as HapMap subjects (0)
C5418626 (UMLS CUI [1,1])
C0549184 (UMLS CUI [1,2])
C0009797 (UMLS CUI [1,3])
C0205257 (UMLS CUI [1,4])
C2700399 (UMLS CUI [1,5])
C0030761 (UMLS CUI [1,6])
C5418626 (UMLS CUI [2,1])
C0549184 (UMLS CUI [2,2])
C0009797 (UMLS CUI [2,3])
C0205257 (UMLS CUI [2,4])
C2700399 (UMLS CUI [2,5])
C0017431 (UMLS CUI [2,6])
C4553389 (UMLS CUI [2,7])
CL Item
Disease-Specific (Prostate Cancer, IRB, NPU, MDS) (DS-PC-IRB-NPU-MDS) (1)
SUBJECT_SOURCE
Item
Subject source
text
C0681850 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
SOURCE_SUBJECT_ID
Item
Source subject ID
text
C2348585 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
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