NIAID Clinical Center Genomics Opportunity (CCGO) Study
Demographics (2)
- SEX - Sex (phv00482398.v1.p1)
- SEX - Sex (phv00482393.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Affection status (phv00483510.v1.p1)
Other (19)
- ANALYTE_TYPE - Analyte type (phv00482410.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00482409.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00482391.v1.p1)
- FAMILY_ID - Family ID (phv00482394.v1.p1)
- FATHER - Father subject ID (phv00482396.v1.p1)
- GENOTYPING_CENTER - Name of the center which conducted genotyping (phv00482412.v1.p1)
- Immunologic deficinecy syndromes - Entrez MeSH-term for primary immune deficiency cohort (phv00482405.v1.p1)
- IS_TUMOR - Tumor status (phv00482411.v1.p1)
- Mastocytosis - Entrez MeSH-term for mastocytosis cohort (phv00482406.v1.p1)
- MOTHER - Mother subject ID (phv00482397.v1.p1)
- Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections - Entrez MeSH-term for PANDAS cohort (phv00482407.v1.p1)
- SAMPLE_ID - De-identified sample ID (phv00482408.v1.p1)
- SAMPLE_ID - Sample ID (phv00482401.v1.p1)
- SAMPLE_USE - Sample Use (phv00482402.v1.p1)
- SIBLING - Sibling subject ID (phv00482399.v1.p1)
- SUBJECT_ID - Unique subject ID (phv00482395.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00482403.v1.p1)
- SUBJECT_ID - Subject ID (phv00482390.v1.p1)
- SUBJECT_ID - Subject ID (phv00482400.v1.p1)