Molecular Etiology of Early-Onset Dystonia
Ancestry (1)
- ancestry - Ancestry of the participant (phv00397063.v1.p1)
Demographics (2)
- Sex - Gender of participant (phv00397060.v1.p1)
- SEX - Sex (phv00397053.v1.p1)
Disease Events (2)
- AFFECTION_STATUS - Case control status of the subject for primary torsin dystonias (phv00397048.v1.p1)
- status - Disease Status of participant (phv00397061.v1.p1)
Other (20)
- ANALYTE_TYPE - Analyte Type (phv00397067.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00397066.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00397045.v1.p1)
- FAMILY_ID - Family ID (phv00397049.v1.p1)
- FATHER - Father's Subject ID (phv00397052.v1.p1)
- inheritance - Type of interitance for disease (phv00397064.v1.p1)
- MOTHER - Mother's Subject ID (phv00397051.v1.p1)
- phenotype - Disease type (phv00397062.v1.p1)
- SAMPLE_ID - Sample ID (phv00397055.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00397065.v1.p1)
- SAMPLE_SOURCE - Source repository where samples originate (phv00397056.v1.p1)
- SAMPLE_USE - Sample Use (phv00397058.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00397068.v1.p1)
- SOURCE_SAMPLE_ID - Sample ID used in the Source Repository (phv00397057.v1.p1)
- SOURCE_SUBJECT_ID - Subject ID used in the Source Repository (phv00397047.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00397059.v1.p1)
- SUBJECT_ID - Subject ID (phv00397044.v1.p1)
- SUBJECT_ID - Unique Subject ID (phv00397050.v1.p1)
- SUBJECT_ID - Subject ID (phv00397054.v1.p1)
- SUBJECT_SOURCE - Source repository where subjects originate (phv00397046.v1.p1)