ID

45454

Beschreibung

Principal Investigator: Richard Lifton, Yale University, New Haven, CT, USA MeSH: Familial Idiopathic Pulmonary Fibrosis,Aortic Coarctation,Aortic Stenosis, Supravalvular,Aortic Valve, Bicuspid,Arteries,Blepharophimosis,Bronchiectasis,Carcinoma, Renal Cell,Cardiomyopathies,Ciliary Motility Disorders,Cleft Palate,Congenital Abnormalities,Diaphragmatic Hernia,Ductus Arteriosus, Patent,Gastroschisis,Heart Defects, Congenital,Heart Septal Defects, Atrial,Heart Valve Diseases,Hemangioma,Hereditary Sensory and Autonomic Neuropathies,Hydrocephalus,Hyper-IgM Immunodeficiency Syndrome,Hyperaldosteronism,Hypertension,Ichthyosiform Erythroderma, Congenital,Idiopathic Pulmonary Fibrosis,Lung Diseases, Interstitial,Muscular Atrophy, Spinal,Neuroblastoma,Pneumothorax,Pulmonary Atresia,Pulmonary Valve Stenosis,Rett Syndrome,Spina Bifida,Tetralogy of Fallot,Transposition of Great Vessels,Tricuspid Atresia https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000744 Yale University is home to one of three national centers created by the NIH to study the genetics of rare inherited diseases. Researchers at Yale, the University of Washington, and a center operated jointly by Baylor and Johns Hopkins University will analyze the genomes of thousands of patients who suffer from more than 6,000 rare Mendelian disorders affecting more than 25 million individuals in US. The Centers for Mendelian Genomics will apply next-generation sequencing and computational approaches to discover the genes and variants that underlie Mendelian disorders. The discovery of new genes that cause Mendelian conditions will expand our understanding about their biology to facilitate their diagnosis, and potentially indicate new treatments. The Centers for Mendelian Genomics will provide free exome sequencing and analysis to collaborating investigators for qualified phenotypes. If you are interested in working with the CMG to discover the genetic basis of a Mendelian condition, please contact Yale Center (shrikant.mane@yale.edu) for further information.

Link

dbGaP-study=phs000744

Stichworte

  1. 11.12.22 11.12.22 - Chiara Middel
Rechteinhaber

Richard Lifton, Yale University, New Haven, CT, USA

Hochgeladen am

11. Dezember 2022

DOI

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Lizenz

Creative Commons BY 4.0

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dbGaP phs000744 Yale Center for Mendelian Genomics (Y CMG)

Sample - Attribute Information

pht003980
Beschreibung

pht003980

Alias
UMLS CUI [1,1]
C3846158
De-identified sequence lab ID of the sample.
Beschreibung

SAMPID

Datentyp

string

Alias
UMLS CUI [1,1]
C2348184
UMLS CUI [1,2]
C4684638
Analyte Type
Beschreibung

ANALYTE_TYPE

Datentyp

string

Alias
UMLS CUI [1,1]
C4744818

Ähnliche Modelle

Sample - Attribute Information

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
pht003980
C3846158 (UMLS CUI [1,1])
SAMPID
Item
De-identified sequence lab ID of the sample.
string
C2348184 (UMLS CUI [1,1])
C4684638 (UMLS CUI [1,2])
ANALYTE_TYPE
Item
Analyte Type
string
C4744818 (UMLS CUI [1,1])

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