Autosomal recessive PGM3 mutations cause a new Congenital Disorder of Glycosylation

AFFECTION_STATUS - Case - control status of the subject (phv00219138.v1.p1)
Allergy - Diagnosis criteria - allergy (phv00219153.v1.p1)
ANALYTE_TYPE - Analyte Type (phv00219159.v1.p1)
Atopic dermatitis - Diagnosis criteria - atopic dermatitis (phv00219154.v1.p1)
BODY_SITE - Body site where sample was collected (phv00219158.v1.p1)
CONSENT - Consent group as determined by DAC (phv00219137.v1.p1)
FAMILY_ID - Family ID (phv00219139.v1.p1)
FATHER - Father's Subject ID (phv00219142.v1.p1)
GENOTYPING_CENTER - Genotyping center (phv00219161.v1.p1)
Infections - Diagnosis criteria - infections (phv00219155.v1.p1)
IS_TUMOR - Tumor status (phv00219160.v1.p1)
MOTHER - Mother's Subject ID (phv00219141.v1.p1)
Neurocognitive impairment - Diagnosis criteria - neurocognitive impairment (phv00219156.v1.p1)
SAMPLE_ID - Sample ID (phv00219146.v1.p1)
SAMPLE_ID - De-identified Sample ID (phv00219157.v1.p1)
SAMPLE_SOURCE - Source repository where samples originate (phv00219147.v1.p1)
SAMPLE_USE - Sample Use (phv00219149.v1.p1)
SOURCE_SAMPLE_ID - Sample ID used at source (phv00219148.v1.p1)
SUBJECT_ID - Unique Subject ID (phv00219140.v1.p1)
SUBJECT_ID - Subject ID (phv00219145.v1.p1)
SUBJECT_ID - Subject ID (phv00219136.v1.p1)
SUBJID - De-identified Subject ID (phv00219150.v1.p1)
TWIN_ID - Twin ID (phv00219144.v1.p1)