Display Settings:

Format

Send to:

Choose Destination
Accession: PRJNA160057 ID: 160057

eMERGE Pediatric Study at CCHMC (human)

See Genome Information for Homo sapiens
This submission includes genotyping data from 6 separate cohorts (named A-E here), each is described in separate paragraphs below. Cohort A) Autism is a neurodevelopmental disorder that affects 1.5 million people in the United States, at an estimated lifetime cost of $4 million. It is part of Pervasive Developmental Disorder characterized by impairments in communication, language and reciprocal social interaction, and by unusual patterns of restricted and repetitive interests or behaviors. Autism, or autistic disorder, is the most severe form of the disease which has a wide range of symptom severity encompassed by the more inclusive term, Autism Spectrum Disorder (ASD). The prevalence of Autistic Disorder is currently estimated to be 4 per 1000, affecting 4 times more boys than girls. More...
AccessionPRJNA160057; dbGaP: phs000494
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 1-Jul-2012
NHGRI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
BioSample4562
Genotype and Phenotype (dbGaP)1
eMERGE Pediatric Study at CCHMC encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA160059Homo sapienseMERGE Pediatric Study at CCHMC (CINCINNATI CHILDRENS HOSP...)

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center