Englisch

Eligibility Criteria

8 Formulare  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for atrial fibrillation (AF).
    3. 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. The data table also includes sample use and substudy accession.
    4. This subject phenotype data table includes subject's sex, race, ethnicity, atrial fibrillation status, age of diagnosis, status at enrollment for age, height, weight, hypertension, diabetes, heart failure, and myocardial infarction. Measurements included are cholesterol (TC, HDL, LDL, and triglycerides) and echocardiogram (PR, QRS, and QT intervals).
    5. This MGH AF CHARGE-S sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    6. This MGH Exome Sequencing in Early AF sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    7. This MGH AF Resequencing sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    8. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and sex of subjects.
Inclusion and exclusion criteria
Beschreibung

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Probands were included if they had a history of atrial fibrillation. In participants with an extensive family history of atrial fibrillation, additional affected and unaffected family members were enrolled.
Beschreibung

Probands were included if they had a history of atrial fibrillation. In participants with an extensive family history of atrial fibrillation, additional affected and unaffected family members were enrolled.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1948021
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0004238
UMLS CUI [2,1]
C0241889
UMLS CUI [2,2]
C0004238
UMLS CUI [2,3]
C2986417
UMLS CUI [2,4]
C0086282
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Ähnliche Modelle

Eligibility Criteria

8 Formulare
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for atrial fibrillation (AF).
    3. 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. The data table also includes sample use and substudy accession.
    4. This subject phenotype data table includes subject's sex, race, ethnicity, atrial fibrillation status, age of diagnosis, status at enrollment for age, height, weight, hypertension, diabetes, heart failure, and myocardial infarction. Measurements included are cholesterol (TC, HDL, LDL, and triglycerides) and echocardiogram (PR, QRS, and QT intervals).
    5. This MGH AF CHARGE-S sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    6. This MGH Exome Sequencing in Early AF sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    7. This MGH AF Resequencing sample attributes table includes body site where sample was collected, analyte type, and tumor status.
    8. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and sex of subjects.
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Probands were included if they had a history of atrial fibrillation. In participants with an extensive family history of atrial fibrillation, additional affected and unaffected family members were enrolled.
Item
Probands were included if they had a history of atrial fibrillation. In participants with an extensive family history of atrial fibrillation, additional affected and unaffected family members were enrolled.
boolean
C1948021 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0241889 (UMLS CUI [2,1])
C0004238 (UMLS CUI [2,2])
C2986417 (UMLS CUI [2,3])
C0086282 (UMLS CUI [2,4])
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