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Clinical VariableDatasetVariable DescriptionVariable ID
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Case control status of the subject for congenital diaphragmatic hernia/defectsphv00420310.v1.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
If the subject has a congenital heart defectphv00301371.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Ethnicity of participantphv00301378.v2.p1
This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Body site where sample was collectedphv00301381.v2.p1
This subject sample mapping file contains 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.
De-identified Subject IDphv00301365.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
De-identified Subject IDphv00301368.v2.p1
This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subjects's sex.
Subject_ID of fatherphv00301362.v2.p1
This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
De-identified Sample IDphv00301380.v2.p1
This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Tumor statusphv00301383.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Other birth defects (1)phv00301374.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Discharge statusphv00301377.v2.p1
This subject consent file includes subject IDs and consent group information.
Consent group as determined by DACphv00301358.v2.p1
This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subjects's sex.
Gender of participantphv00301364.v2.p1
This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subjects's sex.
De-identified Subject IDphv00301361.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Other birth defects (2)phv00301375.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
If the subject has a central nervous system defectphv00301372.v2.p1
This subject sample mapping file contains 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.
De-identified Sample IDphv00301366.v2.p1
This subject phenotype data table includes subject's sex, race, ethnicity, isolated birth defect, congenital heart defect, central nervous system defect, gastrointestinal defect, and other congenital malformations (n=3 variables), discharge status, and affection status for congenital diaphragmatic hernia/defects.
Gender of participantphv00301369.v2.p1
This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Analyte Typephv00301382.v2.p1
This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subjects's sex.
Subject_ID of motherphv00301363.v2.p1
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