organism: Homo sapiens
attributes.tag: gap_accession
attributes.value: phs000707
attributes.tag: submitter handle
attributes.value: NHGRI_Mendelian_HereditaryNeuroDisorders
attributes.tag: biospecimen repository
attributes.value: NHGRI_Mendelian_HereditaryNeuroDisorders
attributes.tag: study name
attributes.value: Next Generation Mendelian Genetics: Hereditary Neurological Disorders
attributes.tag: study design
attributes.value: Case Set
attributes.tag: biospecimen repository sample id
attributes.value: 44848
attributes.tag: submitted sample id
attributes.value: 44848
attributes.tag: submitted subject id
attributes.value: 44848
attributes.tag: gap_sample_id
attributes.value: 2191463
attributes.tag: gap_subject_id
attributes.value: 1819933
attributes.tag: sex
attributes.value: female
attributes.tag: study disease
attributes.value: Nervous System Diseases
attributes.tag: body site
attributes.value: blood
attributes.tag: analyte type
attributes.value: DNA
attributes.tag: subject is affected
attributes.value: Yes
attributes.tag: molecular data type
attributes.value: SNP Genotypes (NGS)
attributes.tag: gap_consent_code
attributes.value: 1
attributes.tag: gap_consent_short_name
attributes.value: DS-HND-NPU