Gene Mutation and Rescue in Human Congenital Diaphragmatic Hernia (CDH)

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Demographics (2)

sex - Gender of participant (phv00217782.v2.p1)
SEX - Sex (phv00290060.v1.p1)

Race and Ethnicity (1)

race - Self Reported Race of participant (phv00217783.v2.p1)

Other (24)

AFFECTION_STATUS - Case control status of the subject for Congenital Diaphragmatic Hernia (CDH) (phv00217775.v2.p1)
ANALYTE_TYPE - Analyte Type (phv00217789.v2.p1)
BODY_SITE - Body site where sample was collected (phv00217788.v2.p1)
cdh_side - Side of diaphragmatic defect (phv00217785.v2.p1)
cdh_type - Type of diaphragmatic hernia (phv00217786.v2.p1)
complex_diaphragmatic_hernia - Whether additional congenital anomalies were reported (phv00217784.v2.p1)
CONSENT - Consent group as determined by DAC (phv00217772.v2.p1)
FAMILY_ID - Family ID (phv00290056.v1.p1)
FATHER - Father's Subject ID (phv00290059.v1.p1)
GENOTYPING_CENTER - Name of the center which conducted genotyping (phv00217791.v2.p1)
IS_TUMOR - Tumor status (phv00217790.v2.p1)
MOTHER - Mother's Subject ID (phv00290058.v1.p1)
SAMPLE_ID - De-identified Sample ID (phv00217787.v2.p1)
SAMPLE_ID - Sample ID (phv00217777.v2.p1)
SAMPLE_SOURCE - Source repository where samples originate (phv00217778.v2.p1)
SAMPLE_USE - Sample use. Seq_DNA_SNP_CNV: SNP and CNV genotypes derived from sequence data; Seq_DNA_WholeExome: Whole exome sequencing (phv00217780.v2.p1)
SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00217792.v2.p1)
SOURCE_SAMPLE_ID - Sample ID used in the Source Repository (phv00217779.v2.p1)
SOURCE_SUBJECT_ID - Subject ID used in the Source Repository (phv00217774.v2.p1)
SUBJECT_ID - De-identified Subject ID (phv00217781.v2.p1)
SUBJECT_ID - Subject ID (phv00217771.v2.p1)
SUBJECT_ID - Subject ID (phv00217776.v2.p1)
SUBJECT_ID - Unique Subject ID (phv00290057.v1.p1)
SUBJECT_SOURCE - Source repository where subjects originate (phv00217773.v2.p1)