ID

45252

Description

Principal Investigator: David Hafler, MD, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA MeSH: Multiple Sclerosis https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000275 The main objective of this GWA study is to identify Multiple Sclerosis (MS) susceptibility loci. Whole-genome association analysis was performed on 924 individuals genotyped on the Affymetrix 6.0 Genechip. The cohort consisted of 860 clinically diagnosed MS patients and 64 control subjects.

Link

dbGaP study = phs000275

Keywords

Versions (2)
  1. 7/4/22 7/4/22 - Chiara Middel
  2. 10/12/22 10/12/22 - Adrian Schulz
Copyright Holder

David Hafler, MD, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

Uploaded on

October 12, 2022

DOI

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License

Creative Commons BY 4.0
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dbGaP phs000275 BWH MS Genetic Collection

English

Pedigree Information

4 forms  
pht002971
Description

pht002971

Unique family identifier
Description

Family_ID

Data type

string

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C2826693
Unique subject identifier
Description

SUBJID

Data type

string

Alias
UMLS CUI [1,1]
C2348585
Unique Paternal ID
Description

Father_ID

Data type

integer

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C0337493
Unique Maternal ID
Description

Mother_ID

Data type

integer

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C1858460
Gender of the participant
Description

Gender

Data type

text

Alias
UMLS CUI [1,1]
C0079399
Diagnosis of the participant
Description

Phenotype

Data type

text

Alias
UMLS CUI [1,1]
C0011900
Corresponding Cel identifier for each subject.
Description

CEL_File_ID

Data type

string

Alias
UMLS CUI [1,1]
C3846158
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Similar models

Pedigree Information

4 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
pht002971
Family_ID
Item
Unique family identifier
string
C0015576 (UMLS CUI [1,1])
C2826693 (UMLS CUI [1,2])
SUBJID
Item
Unique subject identifier
string
C2348585 (UMLS CUI [1,1])
Item
Unique Paternal ID
integer
C2348585 (UMLS CUI [1,1])
C0337493 (UMLS CUI [1,2])
Father_ID
Code List
Unique Paternal ID
CL Item
Missing Paternal ID (0)
C1705492 (UMLS CUI [1,1])
C0337493 (UMLS CUI [1,2])
C2348585 (UMLS CUI [1,3])
Item
Unique Maternal ID
integer
C2348585 (UMLS CUI [1,1])
C1858460 (UMLS CUI [1,2])
Mother_ID
Code List
Unique Maternal ID
CL Item
Missing Maternal ID (0)
C1705492 (UMLS CUI [1,1])
C1858460 (UMLS CUI [1,2])
C2348585 (UMLS CUI [1,3])
Item
Gender of the participant
text
C0079399 (UMLS CUI [1,1])
Gender
Code List
Gender of the participant
CL Item
Male (1)
C0086582 (UMLS CUI [1,1])
CL Item
Female (2)
C0086287 (UMLS CUI [1,1])
Item
Diagnosis of the participant
text
C0011900 (UMLS CUI [1,1])
Phenotype
Code List
Diagnosis of the participant
CL Item
Non MS Control (1)
C0009932 (UMLS CUI [1,1])
C1298908 (UMLS CUI [1,2])
C0026769 (UMLS CUI [1,3])
CL Item
MS (2)
C0026769 (UMLS CUI [1,1])
CEL_File_ID
Item
Corresponding Cel identifier for each subject.
string
C3846158 (UMLS CUI [1,1])
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