Developmental Mechanisms of Human Congenital Heart Disease
Demographics (1)
- SEX - Gender of participant (phv00312976.v1.p1)
Race and Ethnicity (2)
- ETHNICITY - Ethnicity of participant (phv00312978.v1.p1)
- SELF_REPORT_RACE - Race of participant reported by the subject (phv00312977.v1.p1)
Other (19)
- 22q11.2DS - 22q11.2 deletion syndrome (DiGeorge syndrome/velo-cardio-facial syndrome) (phv00312975.v1.p1)
- AFFECTION_STATUS - 22q11DS case control status of the subject for cardiac defect and/or aortic arch anomaly (phv00312968.v1.p1)
- AFFYMETRIX_6_CEL_FILE_ID - Affymetrix 6.0 cel file ID (phv00312972.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00312985.v1.p1)
- BODY_SITE - Body site where sample was taken (phv00312983.v1.p1)
- CELL_LINE - DNA derived from cell line (phv00312984.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00312966.v1.p1)
- GENETIC_DATA_TYPE - Affymetrix (phv00312986.v1.p1)
- HEART_ANOMALY - Intracardiac or aortic arch anomaly (phv00312979.v1.p1)
- PROBAND - Subject with 22q11.2DS (phv00312987.v1.p1)
- PTA - Persistent truncus arteriosus (phv00312980.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00312982.v1.p1)
- SAMPLE_ID - Sample ID (phv00312970.v1.p1)
- SAMPLE_SOURCE - Source research site where samples originate (phv00312971.v1.p1)
- SUBJECT_ID - De-identified subject identification (phv00312974.v1.p1)
- SUBJECT_ID - Subject ID (phv00312965.v1.p1)
- SUBJECT_ID - Subject ID (phv00312969.v1.p1)
- SUBJECT_SOURCE - Source clinical research site where subjects originate (phv00312967.v1.p1)
- TOF - Tetralogy of Fallot (phv00312981.v1.p1)