Undiagnosed Diseases Program (UDP)
Demographics (4)
- AGE - Subject's age (phv00201783.v1.p1)
- SEX - Gender of participant (phv00201781.v1.p1)
- SEX - Sex (phv00201775.v1.p1)
- SEX - Biological sex (phv00487971.v1.p1)
Race and Ethnicity (1)
- RACE - Subject's race (phv00201784.v1.p1)
Other (20)
- AFFECTION_STATUS - Subject's affection status with disease of study (phv00201782.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00201789.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00201788.v1.p1)
- CHIP_TYPE - Type of chip used (phv00201794.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00201770.v1.p1)
- EXOME_CAPTURE_KIT - Name of exome capture kit used for sequencing (phv00201792.v1.p1)
- FAMILY_ID - Family ID (phv00487972.v1.p1)
- FAMILY_ID - Family ID (phv00201771.v1.p1)
- FATHER - Father's Subject ID (phv00201773.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00201790.v1.p1)
- IS_TUMOR - Is tumor? (phv00487974.v1.p1)
- MOTHER - Mother's Subject ID (phv00201774.v1.p1)
- PHENOTYPE - Affected subject's phenotype. See <a href="https://hpo.jax.org/app/">Human Phenotype Ontology (HPO)</a>. (phv00201786.v1.p1)
- REFERENCE_GENOME - Name of reference genome sequence that the sequences were aligned to (phv00201791.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00201787.v1.p1)
- SAMPLE_ID - Sample ID (phv00201777.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00201780.v1.p1)
- SUBJECT_ID - Unique Subject ID (phv00201772.v1.p1)
- SUBJECT_ID - Subject ID (phv00201769.v1.p1)
- SUBJECT_ID - Subject ID (phv00201778.v1.p1)