SAMN01766754
External Id
dbGaP
INSDC center name
2012-10-17T06:23:16.823Z
INSDC first public
2024-05-07T19:49:18.993Z
INSDC last update
SRS390958
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS390958
SRA accession
DNA
analyte type
NHGRI Mendelian Hyperinsulinism
biospecimen repository
5495
biospecimen repository sample id
ARM
http://purl.obolibrary.org/obo/UBERON_0001499
body site
phs000539
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
855762
gap_sample_id
673871
gap_subject_id
BLOOD
http://purl.obolibrary.org/obo/UBERON_0000178
histological type
SNP Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Mendelian
study design
Hyperinsulinism, Congenital
study disease
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
study name
Yes
subject is affected
5495
submitted sample id
5495
submitted subject id
NHGRI Mendelian Hyperinsulinism
submitter handle
DNA sample from ARM of a human male participant in the dbGaP study Next Generation Mendelian Genetics: Congenital Hyperinsulinism
title