ID
36044
Description
Study ID: 100556 (Y11) Clinical Study ID: 100556 Study Title: Long-Term Persistence Follow-up Study to Evaluate the Immune Persistence of GSK Biologicals' Combined Hepatitis A / Hepatitis B Vaccine in Healthy Adult Volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00289718 Sponsor: GlaxoSmithKline Phase: phase 3 Study Recruitment Status: Completed Generic Name: Hepatitis A (Inactivated), Hepatitis B (Recombinant) Vaccine Trade Name: Twinrix Study Indication: Hepatitis A; Hepatitis B
Mots-clés
Versions (1)
- 11/04/2019 11/04/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
11 avril 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Immune Persistence of GSK Biologicals' Combined Hepatitis A / Hepatitis B Vaccine in Healthy Adult Volunteers NCT00289718
Concomitant Vaccination; Medication; Non-Serious Adverse Events; Study Conclusion; Tracking Document; Diary Card
Description
Concomitant Vaccination
Alias
- UMLS CUI-1
- C0042196
- UMLS CUI-2
- C2347852
Description
If yes, please record concomitant vaccination with trade name and/or generic name, route and vaccine administration date.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [2,1]
- C0042210
- UMLS CUI [2,2]
- C3174092
- UMLS CUI [2,3]
- C0332152
- UMLS CUI [3,1]
- C0042210
- UMLS CUI [3,2]
- C0439568
Description
Concomitant Vaccination
Alias
- UMLS CUI-1
- C0042196
- UMLS CUI-2
- C2347852
Description
Trade/ (Generic) Name
Type de données
text
Alias
- UMLS CUI [1]
- C2360065
- UMLS CUI [2]
- C0592502
Description
Route
Type de données
text
Alias
- UMLS CUI [1]
- C0013153
Description
Administration Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1533734
- UMLS CUI [1,2]
- C0011008
Description
Medication
Alias
- UMLS CUI-1
- C0013227
Description
If yes, please complete the following table.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1533734
- UMLS CUI [2,1]
- C0042210
- UMLS CUI [2,2]
- C3174092
- UMLS CUI [2,3]
- C0332152
- UMLS CUI [3,1]
- C0042210
- UMLS CUI [3,2]
- C0439568
Description
Medication
Alias
- UMLS CUI-1
- C0013227
Description
Trade/ Generic Name
Type de données
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C0592502
Description
Medical Indication
Type de données
integer
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0013227
Description
Total daily dose
Type de données
text
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0439810
Description
Medication Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Description
Medication End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Description
Tick box if continuing at end of study
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1553904
- UMLS CUI [1,2]
- C2983670
Description
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Description
If yes, please complete the following table.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C0687676
Description
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Description
Non-Serious Adverse Events Description
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0678257
Description
Non-Serious Adverse Events location
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0450429
Description
Date Non-Serious Adverse Events Started
Type de données
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Description
Non-Serious Adverse Event Start Date during immediate post-vaccination period (30 minutes)
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C0042196
- UMLS CUI [1,4]
- C0687676
- UMLS CUI [1,5]
- C0205253
Description
Date Non-Serious Adverse Event Stopped
Type de données
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Description
Non-Serious Adverse Event Intensity
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Description
Is there a reasonable possibility that the AE may have been caused by the investigational product?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
Description
Non-Serious Adverse Experience Outcome
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
If yes, specify total number of SAE's
Type de données
boolean
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2,1]
- C0042196
- UMLS CUI [2,2]
- C0545082
- UMLS CUI [2,3]
- C1524062
Description
Number of SAE's
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0449788
- UMLS CUI [1,2]
- C1519255
Description
If yes, complete the Pregnancy Notification form.
Type de données
integer
Alias
- UMLS CUI [1]
- C0032961
Description
If yes, record major reason for withdrawal (tick one box only)
Type de données
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
Tick one box only
Type de données
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0392360
Description
Please complete and submit SAE report
Type de données
integer
Description
Please complete Non-serious Adverse Event section
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0237753
- UMLS CUI [2,1]
- C1518404
- UMLS CUI [2,2]
- C0805701
Description
If protocol violation, please specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C2348235
Description
If other reason, please specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C3840932
- UMLS CUI [1,2]
- C2348235
Description
Who made the decision?
Type de données
text
Alias
- UMLS CUI [1]
- C0679006
Description
Date of last contact
Type de données
date
Alias
- UMLS CUI [1]
- C0805839
Description
If No, please give details in Adverse Events section.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1142435
- UMLS CUI [1,2]
- C0681850
Description
Investigator's signature
Alias
- UMLS CUI-1
- C2346576
Description
I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below.
Type de données
text
Alias
- UMLS CUI [1]
- C2346576
Description
Printed Investigator's name
Type de données
text
Alias
- UMLS CUI [1]
- C2826892
Description
Investigator Signature Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Description
Tracking Document - Reason for non participation
Alias
- UMLS CUI-1
- C3889409
- UMLS CUI-2
- C0558080
- UMLS CUI-3
- C0679823
- UMLS CUI-4
- C0392360
Description
Previous subject number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2348585
- UMLS CUI [1,2]
- C0205156
Description
Date of birth
Type de données
date
Alias
- UMLS CUI [1]
- C0421451
Description
Please document reason for non participation
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0558080
- UMLS CUI [1,2]
- C0679823
- UMLS CUI [1,3]
- C0392360
Description
If patient ist not eligible, please specify criteria that are not fulfilled
Type de données
text
Alias
- UMLS CUI [1,1]
- C1555471
- UMLS CUI [1,2]
- C3828770
- UMLS CUI [1,3]
- C2348235
Description
If subject is eligible but not willing to participate, specify reason
Type de données
integer
Alias
- UMLS CUI [1,1]
- C3846156
- UMLS CUI [1,2]
- C0392360
Description
If reason is adverse ebvent or serious adverse event, please specify.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C2348235
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C2348235
Description
If subject is eligible but not willing to participate due to other reason, please specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C3840932
- UMLS CUI [1,2]
- C1521902
- UMLS CUI [1,3]
- C2348568
Description
Subject died on
Type de données
date
Alias
- UMLS CUI [1]
- C1148348
Description
Date of last contact
Type de données
date
Alias
- UMLS CUI [1]
- C0805839
Description
Investigator name (please PRINT name)
Type de données
text
Alias
- UMLS CUI [1]
- C2826892
Description
Signature
Type de données
text
Alias
- UMLS CUI [1]
- C1519316
Description
Date of Signature
Type de données
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Description
Diary Card - Local Symptoms (at injection site)
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Description
Redness ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C3174772
Description
If Redness is ongoing after Day 3, please record Date of last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Description
Please measure the greatest diameter (in mm).
Type de données
integer
Unités de mesure
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Description
Swelling ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C3174772
Description
If Swelling is ongoing after Day 3, record Date of last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Pain intensity - Day 0
Type de données
integer
Alias
- UMLS CUI [1]
- C1320357
Description
Pain intensity - Day 1
Type de données
integer
Alias
- UMLS CUI [1]
- C1320357
Description
Pain intensity - Day 2
Type de données
integer
Alias
- UMLS CUI [1]
- C1320357
Description
Pain intensity - Day 3
Type de données
integer
Alias
- UMLS CUI [1]
- C1320357
Description
Pain ongoing after Day3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C3174772
Description
undefined item
Type de données
date
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Diary Card - Other local symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
- UMLS CUI-4
- C0205394
Description
Description - please specify side(s) and site(s)
Type de données
text
Alias
- UMLS CUI [1]
- C0678257
- UMLS CUI [2,1]
- C0441987
- UMLS CUI [2,2]
- C2348235
- UMLS CUI [3,1]
- C1515974
- UMLS CUI [3,2]
- C2348235
Description
Intensity
Type de données
integer
Alias
- UMLS CUI [1]
- C0518690
Description
Symptom Start date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Description
Symptom End date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Description
Check box if continuing
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Description
Diary Card - Medication
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C3174772
Description
Trade / Generic Name
Type de données
text
Alias
- UMLS CUI [1]
- C2360065
- UMLS CUI [2]
- C0592502
Description
Reason for medication
Type de données
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Description
Total daily dose
Type de données
text
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0439810
Description
Medication Start date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Description
Medication End date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Description
Check box, if medication is continuing
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0549178
Description
Diaray Card - General Symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C0159028
Description
Please record the temperature every day in the evening. If temperature has been taken more than once a day, please report the highest value for the day.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0449687
Description
Temperature - Day 0
Type de données
float
Unités de mesure
- °C
Alias
- UMLS CUI [1]
- C0005903
Description
Temperature - Day 1
Type de données
float
Unités de mesure
- °C
Alias
- UMLS CUI [1]
- C0005903
Description
Temperature - Day 2
Type de données
float
Unités de mesure
- °C
Alias
- UMLS CUI [1]
- C0005903
Description
Temperature - Day 3
Type de données
float
Unités de mesure
- °C
Alias
- UMLS CUI [1]
- C0005903
Description
Temperature ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C3174772
Description
If Temperature is ongoing after Day 3, record Date of last Date of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0549178
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C1517741
- UMLS CUI [1,5]
- C1457887
Description
Fatigue intensity - Day 0
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Description
Fatigue intensity - Day 1
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Description
Fatigue intensity - Day 2
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Description
Fatigue intensity - Day 3
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Description
Fatigue ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C3174772
Description
If Fatigue is ongoing after Day 3, record Date of last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Headache intensity - Day 0
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Description
Headache intensity - Day 1
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Description
Headache intensity - Day 2
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Description
Headache intensity - Day 3
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Description
Is Headache ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C3174772
Description
If Headache is ongoing after Day 3, record Date of last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Gastrointestinal symptoms intensity - Day 0
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Description
Gastrointestinal symptoms intensity - Day 1
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Description
Gastrointestinal symptoms intensity - Day 2
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Description
Gastrointestinal symptoms intensity - Day 3
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Description
Gastrointestinal symptoms ongoing after Day 3?
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C3174772
Description
If Gastrointestinal symptoms are ongoing after Day 3, record Date of last Day of Symptoms
Type de données
date
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Description
Diary Card - Other general Symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C0029625
Description
Description - please give details below
Type de données
text
Alias
- UMLS CUI [1]
- C0678257
- UMLS CUI [2]
- C1522508
Description
Symptom intensity
Type de données
text
Alias
- UMLS CUI [1]
- C0518690
Description
Symptom Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Description
Symptom End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Description
Check box, if symptoms are continuing
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0159028
- UMLS CUI [1,2]
- C0549178
Similar models
Concomitant Vaccination; Medication; Non-Serious Adverse Events; Study Conclusion; Tracking Document; Diary Card
C2347852 (UMLS CUI-2)
C2347852 (UMLS CUI [1,2])
C0042210 (UMLS CUI [2,1])
C3174092 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C0042210 (UMLS CUI [3,1])
C0439568 (UMLS CUI [3,2])
C2347852 (UMLS CUI-2)
C0592502 (UMLS CUI [2])
C0011008 (UMLS CUI [1,2])
C1533734 (UMLS CUI [1,2])
C0042210 (UMLS CUI [2,1])
C3174092 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C0042210 (UMLS CUI [3,1])
C0439568 (UMLS CUI [3,2])
C0592502 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0439810 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C2983670 (UMLS CUI [1,2])
C0042196 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C0678257 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0042196 (UMLS CUI [1,3])
C0687676 (UMLS CUI [1,4])
C0205253 (UMLS CUI [1,5])
C0806020 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0042196 (UMLS CUI [2,1])
C0545082 (UMLS CUI [2,2])
C1524062 (UMLS CUI [2,3])
C1519255 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C1518404 (UMLS CUI [2,1])
C0805701 (UMLS CUI [2,2])
C2348235 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0558080 (UMLS CUI-2)
C0679823 (UMLS CUI-3)
C0392360 (UMLS CUI-4)
C0205156 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C3828770 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C1521902 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0205394 (UMLS CUI-4)
C0441987 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C1515974 (UMLS CUI [3,1])
C2348235 (UMLS CUI [3,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C3174772 (UMLS CUI-2)
C0592502 (UMLS CUI [2])
C0013227 (UMLS CUI [1,2])
C0439810 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0159028 (UMLS CUI-2)
C0449687 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
C1457887 (UMLS CUI [1,5])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C0522510 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C0029625 (UMLS CUI-2)
C1522508 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])