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Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.

6 Formulaires  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    3. Subject ID, sample ID, and sample use of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    4. Subject ID, sample ID, sample source, sample source ID, and sample use of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    5. Subject ID, country of birth, recruitment site, education, sex, visit, study type, affection status of participants [case or control], family history of Alzheimer disease, participant history of diabetes, head injury, heart disease, hypertension, stoke, age at onset, age at examination, age at last examination, allele value of Apolipoprotein E, height and weight, systolic and diastolic blood pressure, color traits, daily living scale, dementia rating scale, score on recognition test, Mattis Dementia Rating Scale, Boston Naming Test, abstract reasoning from WAIS, and smoking status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    6. Sample ID, body site where sample was collected, analyte type, histological type, and tumor status of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
pht003166
Description

pht003166

Subject ID
Description

SUBJID

Type de données

string

Alias
UMLS CUI [1,1]
C2348585
Consent group as determined by CU
Description

CONSENT

Type de données

text

Alias
UMLS CUI [1,1]
C0021430
Subject's Alzheimer's disease affection status
Description

AFFECTION_STATUS

Type de données

text

Alias
UMLS CUI [1,1]
C0002395
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0522476
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Similar models

Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.

6 Formulaires
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    3. Subject ID, sample ID, and sample use of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    4. Subject ID, sample ID, sample source, sample source ID, and sample use of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    5. Subject ID, country of birth, recruitment site, education, sex, visit, study type, affection status of participants [case or control], family history of Alzheimer disease, participant history of diabetes, head injury, heart disease, hypertension, stoke, age at onset, age at examination, age at last examination, allele value of Apolipoprotein E, height and weight, systolic and diastolic blood pressure, color traits, daily living scale, dementia rating scale, score on recognition test, Mattis Dementia Rating Scale, Boston Naming Test, abstract reasoning from WAIS, and smoking status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    6. Sample ID, body site where sample was collected, analyte type, histological type, and tumor status of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
pht003166
SUBJID
Item
Subject ID
string
C2348585 (UMLS CUI [1,1])
Item
Consent group as determined by CU
text
C0021430 (UMLS CUI [1,1])
CONSENT
Code List
Consent group as determined by CU
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)
CL Item
General Research Use (IRB) (GRU-IRB) (1)
Item
Subject's Alzheimer's disease affection status
text
C0002395 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0522476 (UMLS CUI [1,3])
AFFECTION_STATUS
Code List
Subject's Alzheimer's disease affection status
CL Item
Unknown (0)
C0439673 (UMLS CUI [1,1])
CL Item
Not Affected (1)
C0522477 (UMLS CUI [1,1])
CL Item
Affected (2)
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