ID

45454

Beschrijving

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

Trefwoorden

  1. 11-12-22 11-12-22 - Chiara Middel
Houder van rechten

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

Geüploaded op

11 december 2022

DOI

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Licentie

Creative Commons BY 4.0

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dbGaP phs000744 Yale Center for Mendelian Genomics (Y CMG)

Pedigree Information

pht003977
Beschrijving

pht003977

Alias
UMLS CUI [1,1]
C3846158
Sequence Lab ID number, which is de-identified and unique
Beschrijving

SUBJID

Datatype

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348184
Family ID
Beschrijving

FAMID

Datatype

string

Alias
UMLS CUI [1,1]
C3669174
Mother's Subject ID, which is de-identified
Beschrijving

MOTHER

Datatype

string

Alias
UMLS CUI [1,1]
C3669352
UMLS CUI [1,2]
C0030761
UMLS CUI [1,3]
C4684638
Father's Subject ID, which is de-identified
Beschrijving

FATHER

Datatype

string

Alias
UMLS CUI [1,1]
C3669177
UMLS CUI [1,2]
C0030761
UMLS CUI [1,3]
C4684638
Subject's gender
Beschrijving

Sex

Datatype

text

Alias
UMLS CUI [1,1]
C0079399

Similar models

Pedigree Information

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
pht003977
C3846158 (UMLS CUI [1,1])
SUBJID
Item
Sequence Lab ID number, which is de-identified and unique
string
C4684638 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
FAMID
Item
Family ID
string
C3669174 (UMLS CUI [1,1])
MOTHER
Item
Mother's Subject ID, which is de-identified
string
C3669352 (UMLS CUI [1,1])
C0030761 (UMLS CUI [1,2])
C4684638 (UMLS CUI [1,3])
FATHER
Item
Father's Subject ID, which is de-identified
string
C3669177 (UMLS CUI [1,1])
C0030761 (UMLS CUI [1,2])
C4684638 (UMLS CUI [1,3])
Item
Subject's gender
text
C0079399 (UMLS CUI [1,1])
Code List
Subject's gender
CL Item
Female (F)
C0086287 (UMLS CUI [1,1])
CL Item
Male (M)
C0086582 (UMLS CUI [1,1])
CL Item
Unknown (U)
CL Item
Unknown (UNK)

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