Genetics and Functional Studies of Autosomal Recessive Neurological Disorders
Demographics (3)
- AGE - Subject age at enrollment (phv00530386.v1.p1)
- AGE_ONSET - Disease onset age (phv00530387.v1.p1)
- SEX - Biological sex (phv00530381.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case control status of the subject for Intellectual Disability (phv00530388.v1.p1)
Race and Ethnicity (1)
- RACE - Self-reported race (phv00530385.v1.p1)
Other (19)
- ANALYTE_TYPE - Analyte Type (phv00530399.v1.p1)
- Behavioral_anomalies - Behavioral deficits in subject with intellectual disability phenotype (phv00530393.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00530398.v1.p1)
- COLLECTION_AGE - Age sample was collected (phv00530402.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00530380.v1.p1)
- Generalized_Epilepsy - Generalized epilepsy in subject with the intellectual disability phenotype (phv00530390.v1.p1)
- Growth_retardation - Global growth anomalies in subject with intellectual disability phenotype (phv00530394.v1.p1)
- Head_Shape - Microcephaly in subject with the intellectual disability phenotype (phv00530392.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00530401.v1.p1)
- IS_TUMOR - Tumor status (phv00530400.v1.p1)
- Parents_Consangunity - Parent consanguinity of subject with intellectual disability phenotype (phv00530395.v1.p1)
- Phenotype_Severity - Intellectual disability severity status (phv00530389.v1.p1)
- SAMPLE_ID - Sample ID (phv00530397.v1.p1)
- SAMPLE_ID - Sample ID (phv00530383.v1.p1)
- Skeletal_anomalies - Skeletal defects in subject with the intellectual disability phenotype (phv00530391.v1.p1)
- Speech_delay - Speech and language impairment in subject with intellectual disability phenotype (phv00530396.v1.p1)
- SUBJECT_ID - Subject ID (phv00530384.v1.p1)
- SUBJECT_ID - Subject ID (phv00530379.v1.p1)
- SUBJECT_ID - Subject ID (phv00530382.v1.p1)