NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis
Demographics (3)
- Age (in years) - Age at which DNA was acquired (phv00171840.v1.p1)
- sex - Subject sex (phv00171841.v1.p1)
- SEX - Sex (phv00171835.v1.p1)
Disease Events (5)
- AFFECTION_STATUS - Case control status of the subject (phv00171830.v1.p1)
- Bronchiectasis - Presence of Bronchiectasis (phv00171846.v1.p1)
- Neonatal_RDS - Neonatal Respiratory Distress (phv00171844.v1.p1)
- OM - Presence of Otitis Media (phv00171845.v1.p1)
- Sinusitis - Presence of Sinusitis (phv00171847.v1.p1)
Race and Ethnicity (1)
- race - Subject race (phv00171842.v1.p1)
Other (17)
- ANALYTE_TYPE - Analyte Type (phv00171850.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00173104.v1.p1)
- Ciliary_Ultrastructure - Ultrastructural Diagnosis (phv00171843.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00171829.v1.p1)
- FAMID - Family ID (phv00171831.v1.p1)
- FATHER - Father's Subject ID (phv00171834.v1.p1)
- IS_TUMOR - Tumor status (phv00171851.v1.p1)
- MOTHER - Mother's Subject ID (phv00171833.v1.p1)
- NTM - Presence of Nontuberculosis mycobacterium (phv00171848.v1.p1)
- SAMPID - De-identified Sample ID (phv00171849.v1.p1)
- SAMPID - Sample ID (provided by genotyping center) (phv00171838.v1.p1)
- SAMPLE_USE - Sample use. SNP_Sequence: SNP genotypes derived from sequence data; WES_SRA: Whole exome sequencing data available through SRA (phv00172036.v1.p1)
- SUBJID - De-identified Subject ID (phv00171839.v1.p1)
- SUBJID - Unique Subject ID (phv00171832.v1.p1)
- SUBJID - Subject ID (phv00171828.v1.p1)
- SUBJID - Subject ID (phv00171837.v1.p1)
- TWINID - Twin ID (siblings from the same family) (phv00171836.v1.p1)