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This subject phenotype table contains subject IDs, gender, age, primary disease, mutational status of the IgHV genes, and chromosomal alterations as identified by FISH.

4 Formulaires  
pht006065
Description

pht006065

Alias
UMLS CUI [1,1]
C3846158
Unique Participant Identifier
Description

SUBJID

Type de données

string

Alias
UMLS CUI [1,1]
C2348585
Participant's gender as Male or Female
Description

Gender

Type de données

string

Alias
UMLS CUI [1,1]
C0079399
Age of patient
Description

Age

Type de données

string

Unités de mesure
  • years
Alias
UMLS CUI [1,1]
C0001779
years
Primary disease state of patient
Description

Primary Disease

Type de données

string

Alias
UMLS CUI [1,1]
C0205225
UMLS CUI [1,2]
C0012634
UMLS CUI [1,3]
C0449438
Mutational status of the Immunoglobulin Heavy Chain Variable Region Genes (IgHV)
Description

IgHV

Type de données

text

Alias
UMLS CUI [1,1]
C0026882
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C4321381
UMLS CUI [1,4]
C0017337
Chromosomal alterations as identified by Fluorescence in situ Hybridization (FISH)
Description

FISH

Type de données

string

Alias
UMLS CUI [1,1]
C0008625
UMLS CUI [1,2]
C0205396
UMLS CUI [1,3]
C0162789
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Similar models

This subject phenotype table contains subject IDs, gender, age, primary disease, mutational status of the IgHV genes, and chromosomal alterations as identified by FISH.

4 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
pht006065
C3846158 (UMLS CUI [1,1])
SUBJID
Item
Unique Participant Identifier
string
C2348585 (UMLS CUI [1,1])
Item
Participant's gender as Male or Female
string
C0079399 (UMLS CUI [1,1])
Gender
Code List
Participant's gender as Male or Female
CL Item
Female (Female)
C0086287 (UMLS CUI [1,1])
CL Item
Male (Male)
C0086582 (UMLS CUI [1,1])
Age
Item
Age of patient
string
C0001779 (UMLS CUI [1,1])
Item
Primary disease state of patient
string
C0205225 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
Primary Disease
Code List
Primary disease state of patient
CL Item
Chronic Lymphocytic Leukemia (Chronic Lymphocytic Leukemia)
Item
Mutational status of the Immunoglobulin Heavy Chain Variable Region Genes (IgHV)
text
C0026882 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C4321381 (UMLS CUI [1,3])
C0017337 (UMLS CUI [1,4])
IgHV
Code List
Mutational status of the Immunoglobulin Heavy Chain Variable Region Genes (IgHV)
CL Item
Unknown (1)
CL Item
Unmutated (2)
Item
Chromosomal alterations as identified by Fluorescence in situ Hybridization (FISH)
string
C0008625 (UMLS CUI [1,1])
C0205396 (UMLS CUI [1,2])
C0162789 (UMLS CUI [1,3])
FISH
Code List
Chromosomal alterations as identified by Fluorescence in situ Hybridization (FISH)
CL Item
del 11q (del 11q)
CL Item
del 13q, del 11q (del 13q, del 11q)
CL Item
del 17p, del 13q (del 17p, del 13q)
CL Item
del 17p, del 13q, del 11q (del 17p, del 13q, del 11q)
CL Item
del 17p, del 13q, trisomy 12 (del 17p, del 13q, trisomy 12)
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