ID
39433
Beskrivning
Study ID: 111569 Clinical Study ID: 111569 Study Title: A fixed dose, dose-response study for ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01494532 Sponsor: GlaxoSmithKline Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Ropinirole, placebo Study Indication: Parkinson's Disease
Nyckelord
Versioner (2)
- 2019-12-17 2019-12-17 -
- 2020-01-09 2020-01-09 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
9 januari 2020
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Ropinirole prolonged release (PR) as adjunctive treatment to L-Dopa in patients with advanced Parkinson's disease (NCT01494532)
Adverse Events
- StudyEvent: ODM
Beskrivning
Adverse Events
Alias
- UMLS CUI-1
- C0877248
Beskrivning
Diagnosis only, otherwise sign/symptom
Datatyp
text
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
Adverse Event start date - Complete Date Unknown
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2697888
- UMLS CUI [1,2]
- C0439673
Beskrivning
Adverse Event - Start date and time
Datatyp
datetime
Alias
- UMLS CUI [1]
- C2826806
Beskrivning
Adverse Event - Outcome, End date and time
Datatyp
integer
Alias
- UMLS CUI [1]
- C1705586
- UMLS CUI [2]
- C2826793
Beskrivning
Adverse Event end date - Complete Date Unknown
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2826793
- UMLS CUI [1,2]
- C0439673
Beskrivning
Adverse Event - End date/ time
Datatyp
datetime
Alias
- UMLS CUI [1]
- C2826793
Beskrivning
Adverse Event - Frequency
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439603
Beskrivning
Record maximum intensity throughout duration of event
Datatyp
integer
Alias
- UMLS CUI [1]
- C1710066
Beskrivning
Action taken with Investigational Product(s) as a result of the AE
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C0877248
Beskrivning
Please complete the Study Completion Form and Early Withdrawal forms if applicable.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C0877248
Beskrivning
Use best judgement at initial entry. May be amended when additional information becomes available.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beskrivning
Adverse Event - Intensity Changes
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
Beskrivning
Start date and time of event segment change
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C2826806
- UMLS CUI [1,2]
- C0443172
Beskrivning
Intensity of event segment
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0518690
Beskrivning
Was this event serious?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1519255
Beskrivning
Please complete a Possible Suicidality-Related Adverse Event Form
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C3166387
- UMLS CUI [1,3]
- C0332149
Beskrivning
Serious Adverse Event
Alias
- UMLS CUI-1
- C1519255
Beskrivning
Randomisation
Alias
- UMLS CUI-1
- C0034656
Beskrivning
Did SAE occur after initiation of study medication?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
Beskrivning
Record intensity at the onset of event
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0518690
- UMLS CUI [1,2]
- C0332162
Beskrivning
Action taken with Investigational Product(s) as a result of the SAE
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Beskrivning
Please complete the Study Completion Form and Early Withdrawal forms if applicable
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1519255
Beskrivning
Use best judgement at initial entry. May be amended when additional information becomes available
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beskrivning
Duration of AE if <24 hours
Datatyp
integer
Måttenheter
- hr(s)
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0877248
Beskrivning
Duration of AE if <24 hours
Datatyp
integer
Måttenheter
- min(s)
Alias
- UMLS CUI [1,1]
- C0449238
- UMLS CUI [1,2]
- C0877248
Beskrivning
Time to onset since last dose
Datatyp
integer
Måttenheter
- hr(s)
Alias
- UMLS CUI [1,1]
- C0332162
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C3174092
- UMLS CUI [1,4]
- C1517741
Beskrivning
Time to onset since last dose
Datatyp
integer
Måttenheter
- min(s)
Alias
- UMLS CUI [1,1]
- C0332162
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C3174092
- UMLS CUI [1,4]
- C1517741
Beskrivning
Was the SAE caused by activities related to study participation other than investigational product e.g. procedures, blood draws, washout, etc.?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C2348568
- UMLS CUI [3]
- C0304229
- UMLS CUI [4]
- C2700391
- UMLS CUI [5]
- C0005834
- UMLS CUI [6]
- C1710661
- UMLS CUI [7]
- C0439849
Beskrivning
Adverse Event - Seriousness
Alias
- UMLS CUI-1
- C1710056
Beskrivning
Check all that apply
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0392360
Beskrivning
Specify reason for considering this an SAE with general narrative comment
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C2348235
- UMLS CUI [2]
- C0947611
Beskrivning
Relevant Concomitant/Treatment Medications
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0013227
Beskrivning
(Trade name preferred)
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2347946
Beskrivning
Relevant Concomitant/Treatment Medications - Total daily dose
Datatyp
float
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2347946
- UMLS CUI [3,1]
- C2348070
- UMLS CUI [3,2]
- C0439810
Beskrivning
Relevant Concomitant/Treatment Medications - Unit
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2347946
- UMLS CUI [3]
- C0439148
Beskrivning
Relevant Concomitant/Treatment Medications - Indication
Datatyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2347946
- UMLS CUI [3]
- C3146298
Beskrivning
Relevant Concomitant/Treatment Medications - Start date/time
Datatyp
datetime
Alias
- UMLS CUI [1]
- C2826734
- UMLS CUI [2,1]
- C1301880
- UMLS CUI [2,2]
- C2347852
- UMLS CUI [3,1]
- C0013227
- UMLS CUI [3,2]
- C0808070
- UMLS CUI [4,1]
- C0013227
- UMLS CUI [4,2]
- C1301880
Beskrivning
Relevant Concomitant/Treatment Medications - Drug type
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2347946
- UMLS CUI [3]
- C0457591
Beskrivning
Lab Sequence Number
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C2348184
Beskrivning
Relevant Diagnostic Results
Alias
- UMLS CUI-1
- C2347946
- UMLS CUI-2
- C0430022
- UMLS CUI-3
- C0456984
Beskrivning
Test name
Datatyp
text
Alias
- UMLS CUI [1]
- C0022885
Beskrivning
Test date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826247
Beskrivning
Test results
Datatyp
text
Alias
- UMLS CUI [1]
- C0456984
Beskrivning
Test units
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0587081
Beskrivning
Normal low range
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0086715
- UMLS CUI [1,2]
- C0205251
Beskrivning
Normal high range
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0086715
- UMLS CUI [1,2]
- C0205250
Beskrivning
Relevant diagnostic results not noted above
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C0456984
- UMLS CUI [1,3]
- C0205394
Beskrivning
Adverse Events - Rechallenge
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2347900
Beskrivning
If investigational product(s) were stopped temporarily, did the reported event(s) recur after investigational products were restarted?
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1444662
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C0034897
- UMLS CUI [2,3]
- C0580673
Beskrivning
General Narrative Comments
Alias
- UMLS CUI-1
- C0947611
- UMLS CUI-2
- C1135957
Beskrivning
Provide a brief narrative description of SAE, possible other causes of the event e.g. lack of efficacy, withdrawal of investigational product, the disease under study or other medical conditions and details of the treatment
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0947611
- UMLS CUI [1,2]
- C1135957
Beskrivning
Possible suicidality-related adverse event - Section 1
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Possible suicidality-related adverse event - Section 2
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Provide a brief description of the possible suicidality-related AE/SAE
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C3166387
- UMLS CUI [1,3]
- C0678257
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C3166387
- UMLS CUI [2,3]
- C0678257
Beskrivning
Possible suicidality-related adverse event - Section 3
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Disease under study
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Beskrivning
Record in Section 8
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2347852
Beskrivning
Record in Section 8
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0004936
- UMLS CUI [1,2]
- C0009488
Beskrivning
Record in Section 8
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0012634
Beskrivning
Record in Section 8
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0748073
Beskrivning
Withdrawal of investigational product(s)
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C0013227
Beskrivning
Investigational product dose change
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1707811
Beskrivning
Lack of efficacy
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0235828
Beskrivning
Investigational product(s)
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0304229
Beskrivning
Other cause
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0205394
Beskrivning
Specify other cause
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C2348235
Beskrivning
Possible suicidality-related adverse event - Section 4
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Has the subject had any psychiatric conditions in the past (other than the one under study)?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0004936
- UMLS CUI [1,2]
- C0205394
Beskrivning
If subject has had any psychiatric conditions in the past, provide informations
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0004936
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [2]
- C1533716
Beskrivning
Has the subject had any suicidal ideation, behaviour or self-harm in the past?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0424000
- UMLS CUI [1,2]
- C0205156
- UMLS CUI [1,3]
- C1760428
- UMLS CUI [1,4]
- C0424366
Beskrivning
If the subject had any suicidal ideation, behaviour or self-harm in the past, provide information
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0424000
- UMLS CUI [1,2]
- C0205156
- UMLS CUI [1,3]
- C1760428
- UMLS CUI [1,4]
- C0424366
- UMLS CUI [2]
- C1533716
Beskrivning
Subject's current use of illicit drugs?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0281875
- UMLS CUI [1,2]
- C0521116
Beskrivning
If current use of illicit drugs, provide information, including results of a drug screen test if one has been obtained
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0281875
- UMLS CUI [1,2]
- C0521116
- UMLS CUI [2]
- C1533716
- UMLS CUI [3,1]
- C0373483
- UMLS CUI [3,2]
- C1274040
Beskrivning
Subject's current use of alcohol?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0521116
Beskrivning
If current use of alcohol, provide information, including results of an alcohol level test if one has been obtained.
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0521116
- UMLS CUI [2]
- C1533716
- UMLS CUI [3,1]
- C0202304
- UMLS CUI [3,2]
- C1274040
Beskrivning
Family history of suicidality?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0241889
- UMLS CUI [1,2]
- C3166387
Beskrivning
If family history of suicidality, provide information
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0241889
- UMLS CUI [1,2]
- C3166387
- UMLS CUI [2]
- C1533716
Beskrivning
Family history of psychiatric disorders?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0241889
- UMLS CUI [1,2]
- C0004936
Beskrivning
If family history of psychiatric disorders, provide information
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0241889
- UMLS CUI [1,2]
- C0004936
Beskrivning
Possible suicidality-related adverse event - Section 5
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Provide information on the subject's current psycho-social stressors
Datatyp
text
Alias
- UMLS CUI [1]
- C0748073
- UMLS CUI [2]
- C0205409
- UMLS CUI [3]
- C0424960
- UMLS CUI [4]
- C0439849
- UMLS CUI [5]
- C0043227
- UMLS CUI [6]
- C0557159
- UMLS CUI [7]
- C0038435
Beskrivning
Possible suicidality-related adverse event - Section 6
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Provide information on any relevant and/or recent suicidal ideation, not associated with suicidal behaviour, as assessed by the investigator, for this index event
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0424000
- UMLS CUI [1,2]
- C0332185
- UMLS CUI [2]
- C1760428
- UMLS CUI [3]
- C0439603
- UMLS CUI [4]
- C0439793
- UMLS CUI [5]
- C0449238
- UMLS CUI [6]
- C0033204
Beskrivning
Possible suicidality-related adverse event - Section 7
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
For example: Details of any suicidal behaviour, including any plan, preparations, and/or attempt Description of the associated frequencs, severity and duration of these behaviours Likelihood of the subject action upon plans and preparations If possible, description of the subject's intent (or evidence of attention seeking behaviour) Description of the degree of impulsivity or premeditation Description on the subject's mood and thoughts before and after the behaviour
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1760428
- UMLS CUI [1,2]
- C1533716
- UMLS CUI [2,1]
- C0347984
- UMLS CUI [2,2]
- C0008976
Beskrivning
Possible suicidality-related adverse event - Section 8
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2732635
- UMLS CUI-3
- C3166387
Beskrivning
Provide any additional comments or explanation, including but not limited to, both medical and psychiatric treatment, outcome and follow-up.
Datatyp
text
Alias
- UMLS CUI [1]
- C1830770
- UMLS CUI [2,1]
- C0681841
- UMLS CUI [2,2]
- C1524062
- UMLS CUI [3]
- C0237726
- UMLS CUI [4]
- C0204523
- UMLS CUI [5]
- C1547647
- UMLS CUI [6]
- C1522577
Similar models
Adverse Events
- StudyEvent: ODM
C0439673 (UMLS CUI [1,2])
C2826793 (UMLS CUI [2])
C0439673 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0518690 (UMLS CUI-2)
C0392747 (UMLS CUI-3)
C0443172 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C3166387 (UMLS CUI [1,2])
C0332149 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0332162 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0877248 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
C2348568 (UMLS CUI [2])
C0304229 (UMLS CUI [3])
C2700391 (UMLS CUI [4])
C0005834 (UMLS CUI [5])
C1710661 (UMLS CUI [6])
C0439849 (UMLS CUI [7])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0947611 (UMLS CUI [2])
C2347946 (UMLS CUI-2)
C0013227 (UMLS CUI-3)
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C2348070 (UMLS CUI [3,1])
C0439810 (UMLS CUI [3,2])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C0439148 (UMLS CUI [3])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3])
C1301880 (UMLS CUI [2,1])
C2347852 (UMLS CUI [2,2])
C0013227 (UMLS CUI [3,1])
C0808070 (UMLS CUI [3,2])
C0013227 (UMLS CUI [4,1])
C1301880 (UMLS CUI [4,2])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C0457591 (UMLS CUI [3])
C2348184 (UMLS CUI [1,2])
C0430022 (UMLS CUI-2)
C0456984 (UMLS CUI-3)
C0587081 (UMLS CUI [1,2])
C0205251 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,2])
C0456984 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2347900 (UMLS CUI-2)
C1444662 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C0034897 (UMLS CUI [2,2])
C0580673 (UMLS CUI [2,3])
C1135957 (UMLS CUI-2)
C1135957 (UMLS CUI [1,2])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C3166387 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C3166387 (UMLS CUI [2,2])
C0678257 (UMLS CUI [2,3])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0009488 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C1707811 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C1533716 (UMLS CUI [2])
C0205156 (UMLS CUI [1,2])
C1760428 (UMLS CUI [1,3])
C0424366 (UMLS CUI [1,4])
C0205156 (UMLS CUI [1,2])
C1760428 (UMLS CUI [1,3])
C0424366 (UMLS CUI [1,4])
C1533716 (UMLS CUI [2])
C0521116 (UMLS CUI [1,2])
C0521116 (UMLS CUI [1,2])
C1533716 (UMLS CUI [2])
C0373483 (UMLS CUI [3,1])
C1274040 (UMLS CUI [3,2])
C0521116 (UMLS CUI [1,2])
C0521116 (UMLS CUI [1,2])
C1533716 (UMLS CUI [2])
C0202304 (UMLS CUI [3,1])
C1274040 (UMLS CUI [3,2])
C3166387 (UMLS CUI [1,2])
C3166387 (UMLS CUI [1,2])
C1533716 (UMLS CUI [2])
C0004936 (UMLS CUI [1,2])
C0004936 (UMLS CUI [1,2])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C0205409 (UMLS CUI [2])
C0424960 (UMLS CUI [3])
C0439849 (UMLS CUI [4])
C0043227 (UMLS CUI [5])
C0557159 (UMLS CUI [6])
C0038435 (UMLS CUI [7])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C0332185 (UMLS CUI [1,2])
C1760428 (UMLS CUI [2])
C0439603 (UMLS CUI [3])
C0439793 (UMLS CUI [4])
C0449238 (UMLS CUI [5])
C0033204 (UMLS CUI [6])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C1533716 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C2732635 (UMLS CUI-2)
C3166387 (UMLS CUI-3)
C0681841 (UMLS CUI [2,1])
C1524062 (UMLS CUI [2,2])
C0237726 (UMLS CUI [3])
C0204523 (UMLS CUI [4])
C1547647 (UMLS CUI [5])
C1522577 (UMLS CUI [6])