The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)
Demographics (3)
- AGE - Age at Enrollement (phv00487871.v1.p1)
- SEX - Sex (phv00487857.v1.p1)
- SEX - Sex (phv00487852.v1.p1)
Disease Events (1)
- AFFLICTION_STATUS - Whether the subject has been diagnosed with a congenital heart defect (phv00487862.v1.p1)
Race and Ethnicity (1)
- RACE - Race (phv00487870.v1.p1)
Other (24)
- ANALYTE_TYPE - Analyte Type (phv00487875.v1.p1)
- BODY_SITE - Body Site where sample was collected (phv00487873.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00487851.v1.p1)
- FAMILY_ID - Family ID (phv00487854.v1.p1)
- FATHER - Father's Subject ID (phv00487856.v1.p1)
- GENOTYPING_CENTER - Name of the center which conducted genotyping (phv00487877.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00487874.v1.p1)
- MOTHER - Mother's Subject ID (phv00487855.v1.p1)
- MZ_TWIN_ID - Twin ID for monozygotic twins and multiples. An MZ_TWIN_ID is not provided for dizygotic twins or multiples. (phv00487858.v1.p1)
- PHENOTYPE_ID_1 - First ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487863.v1.p1)
- PHENOTYPE_ID_2 - Second ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487864.v1.p1)
- PHENOTYPE_ID_3 - Third ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487865.v1.p1)
- PHENOTYPE_ID_4 - Fourth ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487866.v1.p1)
- PHENOTYPE_ID_5 - Fifth ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487867.v1.p1)
- PHENOTYPE_ID_6 - Sixth ID for a subject's specific diagnosed congenital heart defect. A phenotype ID will not be provided for unaffected subjects. (phv00487868.v1.p1)
- PHENOTYPE_NOTE - Denotes observed phenotype if PHENOTYPE_ID includes 'Other' (phv00487869.v1.p1)
- SAMPLE_ID - Sample ID (phv00493743.v1.p1)
- SAMPLE_ID - Sample ID (phv00487872.v1.p1)
- SAMPLE_ID - Sample ID (phv00487859.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00487876.v1.p1)
- SUBJECT_ID - Subject ID (phv00487861.v1.p1)
- SUBJECT_ID - Subject ID (phv00487853.v1.p1)
- SUBJECT_ID - Subject ID (phv00487850.v1.p1)
- SUBJECT_ID - Subject ID (phv00487860.v1.p1)