ID
36049
Beschrijving
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
Trefwoorden
Versies (5)
- 08-04-19 08-04-19 -
- 08-04-19 08-04-19 -
- 08-04-19 08-04-19 -
- 11-04-19 11-04-19 -
- 20-09-21 20-09-21 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
11 april 2019
DOI
Voor een aanvraag inloggen.
Licentie
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
Long-Term Follow Up (Year 12, Visit 1) - Informed Consent; Demographics; General medical history/ Physical examination; Laboratory Tests; Blood sample conclusion; Vaccine Administration; Unsolicited Adverse Events; Solicited Adverse Events - Local and General Symptoms
Beschrijving
Demographics
Alias
- UMLS CUI-1
- C1704791
Beschrijving
Centre number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0600091
- UMLS CUI [1,2]
- C0019994
Beschrijving
Date of birth
Datatype
date
Alias
- UMLS CUI [1]
- C0421451
Beschrijving
Gender
Datatype
text
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Race
Datatype
integer
Alias
- UMLS CUI [1]
- C0034510
Beschrijving
If other race, please specify
Datatype
text
Alias
- UMLS CUI [1,1]
- C0034510
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C2348235
Beschrijving
General Medical History / Physical Examination
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0031809
Beschrijving
Please tick appropriate box and give diagnosis
Datatype
boolean
Alias
- UMLS CUI [1]
- C0521987
- UMLS CUI [2,1]
- C0037088
- UMLS CUI [2,2]
- C2347804
- UMLS CUI [2,3]
- C0332152
Beschrijving
Medical Condition
Alias
- UMLS CUI-1
- C0012634
Beschrijving
Medical Condition
Datatype
integer
Alias
- UMLS CUI [1]
- C0012634
Beschrijving
Diagnosis
Datatype
text
Alias
- UMLS CUI [1]
- C0011900
Beschrijving
Status
Datatype
integer
Alias
- UMLS CUI [1]
- C0449438
Beschrijving
Laboratory Tests
Alias
- UMLS CUI-1
- C0022885
Beschrijving
Has a blood sample been taken for testing anti-HAV and anti-HBs antibodies?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0201473
- UMLS CUI [2,1]
- C0005834
- UMLS CUI [2,2]
- C0948254
Beschrijving
Please complete only if different from visit date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1277698
- UMLS CUI [1,2]
- C0011008
Beschrijving
Has the subject received since the last visit - A dose of monovalent or combined Hepatitis A or Hepatitis B vaccine?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0170300
- UMLS CUI [1,2]
- C0545082
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1711239
- UMLS CUI [2,1]
- C2240392
- UMLS CUI [2,2]
- C0545082
- UMLS CUI [2,3]
- C1517741
- UMLS CUI [2,4]
- C1711239
Beschrijving
If subject has recieved a dose of monovalent or combined Hepatitis A or Hepatitis B vaccine, please specify
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0170300
- UMLS CUI [1,2]
- C2348235
- UMLS CUI [2,1]
- C2240392
- UMLS CUI [2,2]
- C2348235
Beschrijving
Has the subject received since the last visit - A dose of Hepatitis A or Hepatitis B immunoglobulins within 6 months prior to bleeding?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3652495
- UMLS CUI [1,2]
- C0019080
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [2,1]
- C0062525
- UMLS CUI [2,2]
- C0019080
- UMLS CUI [2,3]
- C0332152
Beschrijving
If subject has received a dose of Hepatitis A or Hepatitis B immunoglobulins within 6 months prior to bleeding, please specify.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3652495
- UMLS CUI [1,2]
- C0019080
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C2348235
- UMLS CUI [2,1]
- C0062525
- UMLS CUI [2,2]
- C0019080
- UMLS CUI [2,3]
- C0332152
- UMLS CUI [2,4]
- C2348235
Beschrijving
Has an additional blood sample been taken prior to additional vaccine dose?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C1524062
- UMLS CUI [2,1]
- C0042210
- UMLS CUI [2,2]
- C0178602
- UMLS CUI [2,3]
- C1524062
Beschrijving
Please complete only if different from visit date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C1524062
- UMLS CUI [1,3]
- C0011008
Beschrijving
HCG Urine Pregnancy Test
Alias
- UMLS CUI-1
- C0430056
Beschrijving
Has a urine sample been taken ?
Datatype
integer
Alias
- UMLS CUI [1]
- C0430056
Beschrijving
Date if different from visit date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0430056
- UMLS CUI [1,2]
- C0011008
Beschrijving
Result
Datatype
integer
Alias
- UMLS CUI [1]
- C1274040
Beschrijving
Blood Sample Conclusion
Alias
- UMLS CUI-1
- C0178913
- UMLS CUI-2
- C1254595
Beschrijving
If yes, please give an additional vaccine dose of Twinrix™ Adult (720/20)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0521144
- UMLS CUI [1,2]
- C0062524
- UMLS CUI [2]
- C0475208
Beschrijving
If yes, please give an additional vaccine dose of either Engerix™ (20 µg) vaccine or Havrix™ (720 EL.U) vaccine
Datatype
text
Alias
- UMLS CUI [1,1]
- C0521144
- UMLS CUI [1,2]
- C0948254
- UMLS CUI [2]
- C0475208
Beschrijving
Vaccine Administration
Alias
- UMLS CUI-1
- C2368628
Beschrijving
fill in only if different from visit date
Datatype
date
Alias
- UMLS CUI [1]
- C0011008
Beschrijving
Pre-Vaccination temperature
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0042196
- UMLS CUI [1,3]
- C0332152
Beschrijving
Temperature Route
Datatype
text
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0449687
Beschrijving
Vaccine Administration
Alias
- UMLS CUI-1
- C2368628
Beschrijving
(only one box must be ticked by vaccine)
Datatype
integer
Alias
- UMLS CUI [1]
- C2368628
Beschrijving
Replacement vial
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0184301
- UMLS CUI [1,2]
- C0559956
- UMLS CUI [1,3]
- C0600091
Beschrijving
Wrong vial number
Datatype
integer
Alias
- UMLS CUI [1]
- C0184301
Beschrijving
Side/ Site Route
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C1515974
- UMLS CUI [1,3]
- C0013153
- UMLS CUI [1,4]
- C0441987
Beschrijving
Has the study vaccine been administered according to the Protocol?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C2348563
Beschrijving
If study vaccine has not been administered according to the Protocol, please tick all items that apply
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C2348563
Beschrijving
Comments
Datatype
text
Alias
- UMLS CUI [1]
- C0947611
Beschrijving
Please tick the ONE most appropriate category for non administration
Datatype
text
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C1272696
Beschrijving
If not administered because of SAE, please specify SAE No.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C1272696
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0237753
Beschrijving
If not administered because of Non-serious Adverse Event, please specify unsolicited or solicited AE No.
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2368628
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C1272696
- UMLS CUI [2,1]
- C1518404
- UMLS CUI [2,2]
- C0237753
Beschrijving
(e.g. consent withdrawal, protocol violation, …)
Datatype
text
Alias
- UMLS CUI [1,1]
- C1533734
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C1272696
- UMLS CUI [1,4]
- C0205394
- UMLS CUI [1,5]
- C2348235
Beschrijving
Please tick who took the decision
Datatype
text
Alias
- UMLS CUI [1]
- C0679006
Beschrijving
Unsolicited Adverse Events
Alias
- UMLS CUI-1
- C0877248
Beschrijving
Has the subject experienced any serious or non-serious unsolicited adverse events during the 30-day (Day 0 to Day 29)post-vaccination?
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0687676
- UMLS CUI [1,3]
- C0042196
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C0687676
- UMLS CUI [2,3]
- C0042196
Beschrijving
Solicited Adverse Events - Local Symptoms
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C1457887
- UMLS CUI-3
- C0205276
Beschrijving
Has the subject experienced any of the following signs/symptoms at the administration site during the solicited period?
Datatype
text
Alias
- UMLS CUI [1,1]
- C0037088
- UMLS CUI [1,2]
- C1515974
- UMLS CUI [1,3]
- C0013153
Beschrijving
Redness
Datatype
boolean
Alias
- UMLS CUI [1]
- C0332575
Beschrijving
Redness size Day 0
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0456389
- UMLS CUI [1,2]
- C0332575
Beschrijving
Redness size Day 1
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0456389
- UMLS CUI [1,2]
- C0332575
Beschrijving
Redness size Day 2
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0456389
- UMLS CUI [1,2]
- C0332575
Beschrijving
Redness size Day 3
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0456389
- UMLS CUI [1,2]
- C0332575
Beschrijving
Redness Ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332575
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Redness is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0332575
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Swelling
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038999
Beschrijving
Swelling Size Day 0
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschrijving
Swelling Size Day 1
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschrijving
Swelling Size Day 2
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschrijving
Swelling Size Day 3
Datatype
integer
Maateenheden
- mm
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C0456389
Beschrijving
Swelling Ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0038999
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Swelling is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0038999
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Pain
Datatype
boolean
Alias
- UMLS CUI [1]
- C0030193
Beschrijving
Pain intensity Day 0
Datatype
integer
Alias
- UMLS CUI [1]
- C1320357
Beschrijving
Pain intensity Day 1
Datatype
integer
Alias
- UMLS CUI [1]
- C1320357
Beschrijving
Pain intensity Day 2
Datatype
integer
Alias
- UMLS CUI [1]
- C1320357
Beschrijving
Pain intensity Day 3
Datatype
integer
Alias
- UMLS CUI [1]
- C1320357
Beschrijving
Pain Ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0030193
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Pain is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0030193
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Solicited Adverse Events - General Symptoms
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0159028
Beschrijving
Has the subject experienced any of the following signs/symptoms during the solicited period?
Datatype
text
Alias
- UMLS CUI [1]
- C0037088
Beschrijving
Axillary > 37.5°C Oral > 37.5°C Rectal > 38° C
Datatype
boolean
Alias
- UMLS CUI [1]
- C0015967
Beschrijving
Temperature Route
Datatype
text
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C0449687
Beschrijving
Temperature Day 0
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschrijving
Temperature not taken Day 0
Datatype
integer
Alias
- UMLS CUI [1]
- C0437722
Beschrijving
Temperature Day 1
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschrijving
Temperature not taken Day 1
Datatype
integer
Alias
- UMLS CUI [1]
- C0437722
Beschrijving
Temperature Day 2
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschrijving
Temperature not taken Day 2
Datatype
integer
Alias
- UMLS CUI [1]
- C0437722
Beschrijving
Temperature Day 3
Datatype
float
Maateenheden
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschrijving
Temperature not taken Day 3
Datatype
integer
Alias
- UMLS CUI [1]
- C0437722
Beschrijving
Fever ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Fever is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0015967
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Fever - Causality?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0015967
- UMLS CUI [1,2]
- C0085978
Beschrijving
Fatigue
Datatype
boolean
Alias
- UMLS CUI [1]
- C0015672
Beschrijving
Fatigue intensity Day 0
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0518690
Beschrijving
Fatigue intensity Day 1
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0518690
Beschrijving
Fatigue intensity Day 2
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0518690
Beschrijving
Fatigue intensity Day 3
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0518690
Beschrijving
Fatigue ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Fatigue is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0015672
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Fatigue - Causality?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0015672
- UMLS CUI [1,2]
- C0085978
Beschrijving
Headache
Datatype
boolean
Alias
- UMLS CUI [1]
- C0018681
Beschrijving
Headache intensity Day 0
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0518690
Beschrijving
Headache intensity Day 1
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0518690
Beschrijving
Headache intensity Day 2
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0518690
Beschrijving
Headache intensity Day 3
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0518690
Beschrijving
Headache ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Headache is ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0018681
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Headache - Causality?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C0085978
Beschrijving
Gastrointestinal symptoms
Datatype
boolean
Alias
- UMLS CUI [1]
- C0426576
Beschrijving
Gastrointestinal symptoms intensity Day 0
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0518690
Beschrijving
Gastrointestinal symptoms intensity Day 1
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0518690
Beschrijving
Gastrointestinal symptoms intensity Day 2
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0518690
Beschrijving
Gastrointestinal symptoms intensity Day 3
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0518690
Beschrijving
Gastrointestinal Symptoms ongoing after Day 3?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C3174772
Beschrijving
If Gastrointestinal symptoms are ongoing, record date of last Day of Symptoms
Datatype
date
Alias
- UMLS CUI [1]
- C0426576
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1517741
- UMLS CUI [2,3]
- C1457887
Beschrijving
Gastrointestinal Symptoms - Causality?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0426576
- UMLS CUI [1,2]
- C0085978
Similar models
Long-Term Follow Up (Year 12, Visit 1) - Informed Consent; Demographics; General medical history/ Physical examination; Laboratory Tests; Blood sample conclusion; Vaccine Administration; Unsolicited Adverse Events; Solicited Adverse Events - Local and General Symptoms
C0019994 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0031809 (UMLS CUI-2)
C0037088 (UMLS CUI [2,1])
C2347804 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C0201473 (UMLS CUI [1,2])
C0005834 (UMLS CUI [2,1])
C0948254 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1711239 (UMLS CUI [1,4])
C2240392 (UMLS CUI [2,1])
C0545082 (UMLS CUI [2,2])
C1517741 (UMLS CUI [2,3])
C1711239 (UMLS CUI [2,4])
C2348235 (UMLS CUI [1,2])
C2240392 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C0019080 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0062525 (UMLS CUI [2,1])
C0019080 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C0019080 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0062525 (UMLS CUI [2,1])
C0019080 (UMLS CUI [2,2])
C0332152 (UMLS CUI [2,3])
C2348235 (UMLS CUI [2,4])
C1524062 (UMLS CUI [1,2])
C0042210 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C1524062 (UMLS CUI [2,3])
C1524062 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C1254595 (UMLS CUI-2)
C0062524 (UMLS CUI [1,2])
C0475208 (UMLS CUI [2])
C0948254 (UMLS CUI [1,2])
C0475208 (UMLS CUI [2])
C0042196 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0559956 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C1515974 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0441987 (UMLS CUI [1,4])
C2348563 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0237753 (UMLS CUI [2,2])
C0392360 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C1518404 (UMLS CUI [2,1])
C0237753 (UMLS CUI [2,2])
C0392360 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0687676 (UMLS CUI [1,2])
C0042196 (UMLS CUI [1,3])
C0877248 (UMLS CUI [2,1])
C0687676 (UMLS CUI [2,2])
C0042196 (UMLS CUI [2,3])
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C1515974 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0332575 (UMLS CUI [1,2])
C0332575 (UMLS CUI [1,2])
C0332575 (UMLS CUI [1,2])
C0332575 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
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 [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C0159028 (UMLS CUI-2)
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C0085978 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C0085978 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C0085978 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C3174772 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
C0085978 (UMLS CUI [1,2])