ID
36044
Beschreibung
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
Stichworte
Versionen (1)
- 11.04.19 11.04.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
11. April 2019
DOI
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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
Beschreibung
Concomitant Vaccination
Alias
- UMLS CUI-1
- C0042196
- UMLS CUI-2
- C2347852
Beschreibung
If yes, please record concomitant vaccination with trade name and/or generic name, route and vaccine administration date.
Datentyp
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
Beschreibung
Concomitant Vaccination
Alias
- UMLS CUI-1
- C0042196
- UMLS CUI-2
- C2347852
Beschreibung
Trade/ (Generic) Name
Datentyp
text
Alias
- UMLS CUI [1]
- C2360065
- UMLS CUI [2]
- C0592502
Beschreibung
Route
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Administration Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1533734
- UMLS CUI [1,2]
- C0011008
Beschreibung
Medication
Alias
- UMLS CUI-1
- C0013227
Beschreibung
If yes, please complete the following table.
Datentyp
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
Beschreibung
Medication
Alias
- UMLS CUI-1
- C0013227
Beschreibung
Trade/ Generic Name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C0592502
Beschreibung
Medical Indication
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0013227
Beschreibung
Total daily dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0439810
Beschreibung
Medication Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beschreibung
Medication End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beschreibung
Tick box if continuing at end of study
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1553904
- UMLS CUI [1,2]
- C2983670
Beschreibung
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Beschreibung
If yes, please complete the following table.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C0687676
Beschreibung
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Beschreibung
Non-Serious Adverse Events Description
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0678257
Beschreibung
Non-Serious Adverse Events location
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0450429
Beschreibung
Date Non-Serious Adverse Events Started
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Beschreibung
Non-Serious Adverse Event Start Date during immediate post-vaccination period (30 minutes)
Datentyp
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
Beschreibung
Date Non-Serious Adverse Event Stopped
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beschreibung
Non-Serious Adverse Event Intensity
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Beschreibung
Is there a reasonable possibility that the AE may have been caused by the investigational product?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
Beschreibung
Non-Serious Adverse Experience Outcome
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beschreibung
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Beschreibung
If yes, specify total number of SAE's
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2,1]
- C0042196
- UMLS CUI [2,2]
- C0545082
- UMLS CUI [2,3]
- C1524062
Beschreibung
Number of SAE's
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0449788
- UMLS CUI [1,2]
- C1519255
Beschreibung
If yes, complete the Pregnancy Notification form.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0032961
Beschreibung
If yes, record major reason for withdrawal (tick one box only)
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschreibung
Tick one box only
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0392360
Beschreibung
Please complete and submit SAE report
Datentyp
integer
Beschreibung
Please complete Non-serious Adverse Event section
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0237753
- UMLS CUI [2,1]
- C1518404
- UMLS CUI [2,2]
- C0805701
Beschreibung
If protocol violation, please specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C2348235
Beschreibung
If other reason, please specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3840932
- UMLS CUI [1,2]
- C2348235
Beschreibung
Who made the decision?
Datentyp
text
Alias
- UMLS CUI [1]
- C0679006
Beschreibung
Date of last contact
Datentyp
date
Alias
- UMLS CUI [1]
- C0805839
Beschreibung
If No, please give details in Adverse Events section.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1142435
- UMLS CUI [1,2]
- C0681850
Beschreibung
Investigator's signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Printed Investigator's name
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Beschreibung
Investigator Signature Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beschreibung
Tracking Document - Reason for non participation
Alias
- UMLS CUI-1
- C3889409
- UMLS CUI-2
- C0558080
- UMLS CUI-3
- C0679823
- UMLS CUI-4
- C0392360
Beschreibung
Previous subject number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2348585
- UMLS CUI [1,2]
- C0205156
Beschreibung
Date of birth
Datentyp
date
Alias
- UMLS CUI [1]
- C0421451
Beschreibung
Please document reason for non participation
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0558080
- UMLS CUI [1,2]
- C0679823
- UMLS CUI [1,3]
- C0392360
Beschreibung
If patient ist not eligible, please specify criteria that are not fulfilled
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1555471
- UMLS CUI [1,2]
- C3828770
- UMLS CUI [1,3]
- C2348235
Beschreibung
If subject is eligible but not willing to participate, specify reason
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C3846156
- UMLS CUI [1,2]
- C0392360
Beschreibung
If reason is adverse ebvent or serious adverse event, please specify.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C2348235
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C2348235
Beschreibung
If subject is eligible but not willing to participate due to other reason, please specify
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3840932
- UMLS CUI [1,2]
- C1521902
- UMLS CUI [1,3]
- C2348568
Beschreibung
Subject died on
Datentyp
date
Alias
- UMLS CUI [1]
- C1148348
Beschreibung
Date of last contact
Datentyp
date
Alias
- UMLS CUI [1]
- C0805839
Beschreibung
Investigator name (please PRINT name)
Datentyp
text
Alias
- UMLS CUI [1]
- C2826892
Beschreibung
Signature
Datentyp
text
Alias
- UMLS CUI [1]
- C1519316
Beschreibung
Date of Signature
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Beschreibung
Diary Card - Local Symptoms (at injection site)
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0456389
Beschreibung
Redness ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Redness is ongoing after Day 3, please record Date of last Day of Symptoms
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschreibung
Please measure the greatest diameter (in mm).
Datentyp
integer
Maßeinheiten
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschreibung
Swelling ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Swelling is ongoing after Day 3, record Date of last Day of Symptoms
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Pain intensity - Day 0
Datentyp
integer
Alias
- UMLS CUI [1]
- C1320357
Beschreibung
Pain intensity - Day 1
Datentyp
integer
Alias
- UMLS CUI [1]
- C1320357
Beschreibung
Pain intensity - Day 2
Datentyp
integer
Alias
- UMLS CUI [1]
- C1320357
Beschreibung
Pain intensity - Day 3
Datentyp
integer
Alias
- UMLS CUI [1]
- C1320357
Beschreibung
Pain ongoing after Day3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C3174772
Beschreibung
undefined item
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Diary Card - Other local symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
- UMLS CUI-4
- C0205394
Beschreibung
Description - please specify side(s) and site(s)
Datentyp
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
Beschreibung
Intensity
Datentyp
integer
Alias
- UMLS CUI [1]
- C0518690
Beschreibung
Symptom Start date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Beschreibung
Symptom End date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Beschreibung
Check box if continuing
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C3174772
Beschreibung
Diary Card - Medication
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C3174772
Beschreibung
Trade / Generic Name
Datentyp
text
Alias
- UMLS CUI [1]
- C2360065
- UMLS CUI [2]
- C0592502
Beschreibung
Reason for medication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Beschreibung
Total daily dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0439810
Beschreibung
Medication Start date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0808070
Beschreibung
Medication End date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0806020
Beschreibung
Check box, if medication is continuing
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0549178
Beschreibung
Diaray Card - General Symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C0159028
Beschreibung
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.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0449687
Beschreibung
Temperature - Day 0
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Temperature - Day 1
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Temperature - Day 2
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Temperature - Day 3
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Temperature ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Temperature is ongoing after Day 3, record Date of last Date of Symptoms
Datentyp
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
Beschreibung
Fatigue intensity - Day 0
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Beschreibung
Fatigue intensity - Day 1
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Beschreibung
Fatigue intensity - Day 2
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Beschreibung
Fatigue intensity - Day 3
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0522510
Beschreibung
Fatigue ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Fatigue is ongoing after Day 3, record Date of last Day of Symptoms
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Headache intensity - Day 0
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Beschreibung
Headache intensity - Day 1
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Beschreibung
Headache intensity - Day 2
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Beschreibung
Headache intensity - Day 3
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0522510
Beschreibung
Is Headache ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Headache is ongoing after Day 3, record Date of last Day of Symptoms
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Gastrointestinal symptoms intensity - Day 0
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Beschreibung
Gastrointestinal symptoms intensity - Day 1
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Beschreibung
Gastrointestinal symptoms intensity - Day 2
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Beschreibung
Gastrointestinal symptoms intensity - Day 3
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0522510
Beschreibung
Gastrointestinal symptoms ongoing after Day 3?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C3174772
Beschreibung
If Gastrointestinal symptoms are ongoing after Day 3, record Date of last Day of Symptoms
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1457887
Beschreibung
Diary Card - Other general Symptoms
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C0029625
Beschreibung
Description - please give details below
Datentyp
text
Alias
- UMLS CUI [1]
- C0678257
- UMLS CUI [2]
- C1522508
Beschreibung
Symptom intensity
Datentyp
text
Alias
- UMLS CUI [1]
- C0518690
Beschreibung
Symptom Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0808070
Beschreibung
Symptom End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1457887
- UMLS CUI [1,2]
- C0806020
Beschreibung
Check box, if symptoms are continuing
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0159028
- UMLS CUI [1,2]
- C0549178
Ähnliche Modelle
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])