SAMN01766752
External Id
dbGaP
INSDC center name
2012-10-17T06:23:16.487Z
INSDC first public
2024-05-07T19:49:18.333Z
INSDC last update
SRS390959
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS390959
SRA accession
DNA
analyte type
NHGRI Mendelian Hyperinsulinism
biospecimen repository
5492
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
855760
gap_sample_id
673869
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
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Mendelian
study design
Hyperinsulinism, Congenital
study disease
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
study name
Yes
subject is affected
5492
submitted sample id
5492
submitted subject id
NHGRI Mendelian Hyperinsulinism
submitter handle
DNA sample from ARM of a human female participant in the dbGaP study Next Generation Mendelian Genetics: Congenital Hyperinsulinism
title