Next Generation Mendelian Genetics: Hereditary Neurological Disorders
Demographics (1)
- SEX - Sex (phv00200320.v2.p1)
Disease Events (2)
- AFFECTION_STATUS - Case - control status of the subject (phv00200322.v2.p1)
- CONDITION - Name of disorder; presumed or confirmed. (phv00200323.v2.p1)
Race and Ethnicity (1)
- RACE - Race of participant (phv00200321.v2.p1)
Other (13)
- ANALYTE_TYPE - Analyte type (phv00200327.v2.p1)
- BODY_SITE - Body site where sample was collected (phv00200326.v2.p1)
- CONSENT - Consent group as determined by DAC (phv00200315.v2.p1)
- FAMID - De-identified family ID (phv00283712.v1.p1)
- RELATEDNESS - Familial relationships (phv00283713.v1.p1)
- SAMPID - De-identified Sample ID (phv00200317.v2.p1)
- SAMPID - De-identified Sample ID (phv00200325.v2.p1)
- SAMPLE_SOURCE - Sample source (phv00283710.v1.p1)
- SAMPLE_USE - Use of samples. Seq_DNA_SNP: SNP genotypes derived from sequence data; Seq_DNA_WholeExome: Whole exome sequencing (phv00200318.v2.p1)
- SOURCE_SAMPLE_ID - De-identified Source Sample ID (phv00283711.v1.p1)
- SUBJID - De-identified Subject ID (phv00200319.v2.p1)
- SUBJID - De-identified Subject ID (phv00200316.v2.p1)
- SUBJID - De-identified Subject ID (phv00200314.v2.p1)