ID
43936
Beschreibung
XELODA and Lapatinib Advanced or Metastatic Breast Cancer Study ID: 100151 Clinical Study ID: EGF100151 Study Title: A Phase III, Randomized, Open-label, Multicenter Study Comparing GW572016 and Capecitabine (XELODA) versus Capecitabine in Women with Refractory Advanced or Metastatic Breast Cancer Clinicaltrials.gov Identifier: NCT00078572 https://clinicaltrials.gov/ct2/show/NCT00078572 Procedure: Screening Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lapatinib Trade Name: Tyverb,Tykerb,Tycerb Study Indication: Breast Cancer; Neoplasms, Breast
Link
https://clinicaltrials.gov/ct2/show/NCT00078572
Stichworte
Versionen (2)
- 29.05.17 29.05.17 -
- 20.09.21 20.09.21 -
Hochgeladen am
20. September 2021
DOI
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Lizenz
Creative Commons BY-NC 3.0
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XELODA and Lapatinib Advanced or Metastatic Breast Cancer Screening NCT00078572
XELODA and Lapatinib Advanced or Metastatic Breast Cancer Screening NCT00078572
Beschreibung
Pharmacogenetic Research - Tumor - Informed Consent
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C0006826
Beschreibung
informed consent
Datentyp
text
Alias
- UMLS CUI [1]
- C0021430
Beschreibung
Date informed consent obtained
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0514044
- UMLS CUI [1,2]
- C0011008
Beschreibung
reason informed consent was not obtained
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1705116
- UMLS CUI [1,3]
- C0392360
Beschreibung
tumor sample
Datentyp
text
Alias
- UMLS CUI [1]
- C0475358
Beschreibung
Date tumor sample taken
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0475358
Beschreibung
withdraw consent
Datentyp
text
Alias
- UMLS CUI [1]
- C2349954
Beschreibung
Inclusion Criteria Worksheet
Alias
- UMLS CUI-1
- C1512693
- UMLS CUI-2
- C1516637
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0021430
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0853879
- UMLS CUI [2]
- C0278488
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1515559
- UMLS CUI [1,2]
- C0587081
- UMLS CUI [2]
- C0853879
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study. NOTE: Progression for entry is defined as appearance of any new lesion not previously identified or increase of 25% or more in existent lesions and must be documented.
Datentyp
text
Alias
- UMLS CUI [1]
- C0278488
- UMLS CUI [2]
- C0853879
Beschreibung
Check YES if this is applicable for the subject.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0678222
- UMLS CUI [1,2]
- C0205269
Beschreibung
Check YES if this is applicable for the subject.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0728747
Beschreibung
Check YES if this is applicable for the subject, otherwise check NO.
Datentyp
text
Alias
- UMLS CUI [1]
- C1563119
- UMLS CUI [2]
- C0242656
- UMLS CUI [3]
- C0279025
Beschreibung
Check YES if this is applicable for the subject
Datentyp
text
Alias
- UMLS CUI [1]
- C0686377
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0001779
- UMLS CUI [1,2]
- C0681850
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C1520224
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1513041
- UMLS CUI [1,2]
- C1709926
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0003738
- UMLS CUI [1,2]
- C0475358
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0023671
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C2004454
- UMLS CUI [2,1]
- C0001688
- UMLS CUI [2,2]
- C1522449
- UMLS CUI [3,1]
- C0001688
- UMLS CUI [3,2]
- C0392920
Beschreibung
Check YES if this is applicable for the subject
Datentyp
text
Alias
- UMLS CUI [1]
- C1522449
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0232174
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0175795
- UMLS CUI [1,2]
- C2712086
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C1710477
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0232804
Beschreibung
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0221130
- UMLS CUI [2]
- C0232741
Beschreibung
Exclusion Criteria Worksheet
Alias
- UMLS CUI-1
- C0680251
Beschreibung
Exclusion Criteria check one box for each question: If any EXCLUSION CRITERIA question is answered YES, this subject must NOT enter this study.
Datentyp
text
Alias
- UMLS CUI [1]
- C0549206
Beschreibung
Malabsorption Syndrome, disease significantly affecting gastrointestinal function, resection of the stomach or small bowel, or ulcerative colitis
Datentyp
text
Alias
- UMLS CUI [1]
- C0024523
- UMLS CUI [2]
- C0017178
Beschreibung
history of other malignancy
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0027651
- UMLS CUI [1,2]
- C0262926
Beschreibung
concurrent disease or condition
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C1548788
Beschreibung
unresolved or unstable, serious toxicity
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0013221
- UMLS CUI [1,2]
- C0013230
Beschreibung
active or uncontrolled infection
Datentyp
text
Alias
- UMLS CUI [1]
- C0009450
Beschreibung
dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Beschreibung
history of uncontrolled or symptomatic angina, arrhythmias, or congestive heart failure
Datentyp
text
Alias
- UMLS CUI [1]
- C0018799
Beschreibung
coumarin-derivative anticoagulants
Datentyp
text
Alias
- UMLS CUI [1]
- C0003280
- UMLS CUI [2]
- C0010207
Beschreibung
history of, or clinical evidence of leptomeningeal carcinomatosis
Datentyp
text
Alias
- UMLS CUI [1]
- C0220654
Beschreibung
concurrent anti-cancer therapy other than capecitabine
Datentyp
text
Alias
- UMLS CUI [1]
- C0920425
Beschreibung
Check NO if this is applicable for the subject
Datentyp
text
Alias
- UMLS CUI [1]
- C0012544
Beschreibung
concurrent treatment with an investigational agent or participating in another clinical trial
Datentyp
text
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
Beschreibung
used an investigational drug
Datentyp
text
Alias
- UMLS CUI [1]
- C0013230
Beschreibung
immediate or delayed hypersensitivity reaction or idiosyncrasy
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1384663
- UMLS CUI [2,1]
- C0231191
- UMLS CUI [2,2]
- C1384663
Beschreibung
immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to capecitabine, fluorouracil or any excipients?
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0231191
- UMLS CUI [2,1]
- C0671970
- UMLS CUI [2,2]
- C0016360
- UMLS CUI [2,3]
- C0015237
Beschreibung
dihydropyrimidine dehydrogenase (DPD) deficiency
Datentyp
text
Alias
- UMLS CUI [1]
- C1959620
Beschreibung
Inclusion and Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
- UMLS CUI-2
- C1512693
- UMLS CUI-3
- C1516637
Beschreibung
Protocol code
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1507394
- UMLS CUI [1,2]
- C0600091
Beschreibung
Session number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1883017
- UMLS CUI [1,2]
- C0750480
Beschreibung
Subject number
Datentyp
text
Alias
- UMLS CUI [1]
- C2348585
Beschreibung
meet all entry criteria
Datentyp
text
Alias
- UMLS CUI [1]
- C0013893
Beschreibung
violation of the inclusion criteria
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C1512693
- UMLS CUI [2]
- C1516637
Beschreibung
violation of the exclusion criteria
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C0680251
- UMLS CUI [2]
- C1516637
Beschreibung
Current Medical Conditions / Baseline Signs and Symptoms
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0012634
- UMLS CUI-3
- C1457887
Beschreibung
current medical conditions, baseline signs or symptoms
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1457887
Beschreibung
If YES, record all screening clinical signs and symptoms below according to the instructions on the facing page.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1457887
Beschreibung
Refer to the NCI CTCAE Common Toxicity Criteria version 3 in the study reference manual. If the condition is not found in the NCI CTCAE, assign a grade using one of the following: 1=Mild, 2=Moderate, 3=Severe, 4=Life Threatening
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C3887242
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C1457887
Beschreibung
Physical Exam (Vital Signs, Weight, Height)
Alias
- UMLS CUI-1
- C0518766
Beschreibung
NOTE: Record Vital Signs within 2 weeks prior to first dose of medication NOTE: Blood pressure and heart rate must be taken after 5 minutes of sitting
Datentyp
date
Alias
- UMLS CUI [1]
- C0011008
Beschreibung
Blood pressure systolic
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschreibung
Blood pressure diastolic
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Heart rate
Datentyp
integer
Maßeinheiten
- beats/min
Alias
- UMLS CUI [1]
- C0018810
Beschreibung
Height
Datentyp
integer
Maßeinheiten
- cm
Alias
- UMLS CUI [1]
- C0005890
Beschreibung
Weight
Datentyp
float
Maßeinheiten
- kg
Alias
- UMLS CUI [1]
- C0005910
Beschreibung
Temperature
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
ECOG Performance Status
Alias
- UMLS CUI-1
- C1520224
Beschreibung
Cardiac Assessments Screening
Alias
- UMLS CUI-1
- C1623258
- UMLS CUI-2
- C0013516
Beschreibung
If NO, record details on the INVESTIGATOR COMMENT LOG page. If YES, record details below.
Datentyp
text
Alias
- UMLS CUI [1]
- C0430456
Beschreibung
Date of assessment
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1623258
Beschreibung
ECG results
Datentyp
text
Alias
- UMLS CUI [1]
- C1623258
Beschreibung
If YES, record the abnormality on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page at Screening.
Datentyp
text
Alias
- UMLS CUI [1]
- C1623258
Beschreibung
If YES, record details below.
Datentyp
text
Alias
- UMLS CUI [1]
- C0013516
Beschreibung
Institution name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0013516
Beschreibung
Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0013516
Beschreibung
Left ventricular ejection fraction
Datentyp
integer
Maßeinheiten
- %
Alias
- UMLS CUI [1]
- C0428772
- UMLS CUI [2]
- C0013516
Beschreibung
Lower limit of normal
Datentyp
integer
Maßeinheiten
- %
Alias
- UMLS CUI [1,1]
- C1518030
- UMLS CUI [1,2]
- C0428772
- UMLS CUI [2]
- C0013516
Beschreibung
If YES, record details below.
Datentyp
text
Alias
- UMLS CUI [1]
- C0521317
Beschreibung
Institution name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0521317
Beschreibung
Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0521317
Beschreibung
Left ventricular ejection fraction
Datentyp
integer
Maßeinheiten
- %
Alias
- UMLS CUI [1]
- C0428772
- UMLS CUI [2]
- C0521317
Beschreibung
NOTE: If left ventricular ejection fraction is not within institutional range of normal, the subject must not enter the study.
Datentyp
integer
Maßeinheiten
- %
Alias
- UMLS CUI [1,1]
- C1518030
- UMLS CUI [1,2]
- C0428772
- UMLS CUI [2]
- C0521317
Beschreibung
Hematology - Local Lab Screening
Alias
- UMLS CUI-1
- C0474523
Beschreibung
Any clinically significant laboratory abnormalities must be recorded on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0022877
- UMLS CUI [1,2]
- C0600091
Beschreibung
Lab name
Datentyp
text
Alias
- UMLS CUI [1]
- C1882331
Beschreibung
Date hematology sample taken
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [2]
- C0474523
Beschreibung
Units
Datentyp
integer
Alias
- UMLS CUI [1]
- C1519795
Beschreibung
Hemoglobin
Datentyp
float
Alias
- UMLS CUI [1]
- C0518015
Beschreibung
Hematocrit
Datentyp
float
Alias
- UMLS CUI [1]
- C0518014
Beschreibung
RBC
Datentyp
integer
Alias
- UMLS CUI [1]
- C0014772
Beschreibung
Platelets
Datentyp
integer
Alias
- UMLS CUI [1]
- C0032181
Beschreibung
Total WBC
Datentyp
integer
Alias
- UMLS CUI [1]
- C0023508
Beschreibung
Neutrophils
Datentyp
integer
Alias
- UMLS CUI [1]
- C0948762
Beschreibung
Granulocytes
Datentyp
integer
Alias
- UMLS CUI [1]
- C0857490
Beschreibung
Lymphocytes
Datentyp
integer
Alias
- UMLS CUI [1]
- C0200635
Beschreibung
Monocytes
Datentyp
integer
Alias
- UMLS CUI [1]
- C0200637
Beschreibung
Eosinophils
Datentyp
integer
Alias
- UMLS CUI [1]
- C0200638
Beschreibung
Basophils
Datentyp
integer
Alias
- UMLS CUI [1]
- C0200641
Beschreibung
Clinical Chemistry - Local Lab Screening
Alias
- UMLS CUI-1
- C2347783
Beschreibung
Any clinically significant laboratory abnormalities must be recorded on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0022877
- UMLS CUI [1,2]
- C0600091
Beschreibung
Lab name
Datentyp
text
Alias
- UMLS CUI [1]
- C1882331
Beschreibung
Date clinical chemistry sample taken
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [2]
- C2347783
Beschreibung
Sodium
Datentyp
float
Alias
- UMLS CUI [1]
- C0337443
Beschreibung
Potassium
Datentyp
float
Alias
- UMLS CUI [1]
- C0202194
Beschreibung
Chloride
Datentyp
float
Alias
- UMLS CUI [1]
- C0201952
Beschreibung
Bicarbonate
Datentyp
float
Alias
- UMLS CUI [1]
- C0202059
Beschreibung
Calcium
Datentyp
float
Alias
- UMLS CUI [1]
- C0201925
Beschreibung
Glucose
Datentyp
float
Alias
- UMLS CUI [1]
- C0202042
Beschreibung
Total Protein
Datentyp
float
Alias
- UMLS CUI [1]
- C0555903
Beschreibung
Albumin
Datentyp
float
Alias
- UMLS CUI [1]
- C0201838
Beschreibung
Uric acid
Datentyp
float
Alias
- UMLS CUI [1]
- C0202239
Beschreibung
Creatinine
Datentyp
float
Alias
- UMLS CUI [1]
- C0201976
Beschreibung
BUN
Datentyp
float
Alias
- UMLS CUI [1]
- C0005845
Beschreibung
Urea
Datentyp
float
Alias
- UMLS CUI [1]
- C0523961
Beschreibung
Total bilirubin
Datentyp
float
Alias
- UMLS CUI [1]
- C0201913
Beschreibung
Alkaline phosphatase
Datentyp
float
Alias
- UMLS CUI [1]
- C0201850
Beschreibung
AST (SGOT)
Datentyp
float
Alias
- UMLS CUI [1]
- C0201899
Beschreibung
ALT (SGPT)
Datentyp
float
Alias
- UMLS CUI [1]
- C0201836
Beschreibung
NOTE: Refer to the creatinine clearance worksheet for calculation.
Datentyp
float
Alias
- UMLS CUI [1]
- C0373595
Beschreibung
Creatinine Clearance Worksheet
Datentyp
float
Maßeinheiten
- kg
Alias
- UMLS CUI [1]
- C0005910
Beschreibung
Creatinine Clearance Worksheet
Datentyp
integer
Maßeinheiten
- cm
Alias
- UMLS CUI [1]
- C0005890
Beschreibung
Creatinine Clearance Worksheet
Datentyp
integer
Maßeinheiten
- years
Alias
- UMLS CUI [1]
- C0001779
Beschreibung
Creatinine Clearance Worksheet
Datentyp
float
Alias
- UMLS CUI [1]
- C0201976
Beschreibung
Creatinine Clearance Worksheet
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0201976
- UMLS CUI [1,2]
- C1519795
Ähnliche Modelle
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C0005767 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C1272683 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0006826 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,2])
C0475358 (UMLS CUI [1,3])
C1516637 (UMLS CUI-2)
C0278488 (UMLS CUI [2])
C0587081 (UMLS CUI [1,2])
C0853879 (UMLS CUI [2])
C0853879 (UMLS CUI [2])
C0205269 (UMLS CUI [1,2])
C0728747 (UMLS CUI [1,2])
C0242656 (UMLS CUI [2])
C0279025 (UMLS CUI [3])
C0681850 (UMLS CUI [1,2])
C1709926 (UMLS CUI [1,2])
C0475358 (UMLS CUI [1,2])
C0001688 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C0001688 (UMLS CUI [3,1])
C0392920 (UMLS CUI [3,2])
C2712086 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0017178 (UMLS CUI [2])
C0262926 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0013230 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0010207 (UMLS CUI [2])
C0013230 (UMLS CUI [2])
C1384663 (UMLS CUI [1,2])
C0231191 (UMLS CUI [2,1])
C1384663 (UMLS CUI [2,2])
C0231191 (UMLS CUI [1,2])
C0671970 (UMLS CUI [2,1])
C0016360 (UMLS CUI [2,2])
C0015237 (UMLS CUI [2,3])
C1512693 (UMLS CUI-2)
C1516637 (UMLS CUI-3)
C0600091 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,2])
C1516637 (UMLS CUI [2])
C0680251 (UMLS CUI [1,2])
C1516637 (UMLS CUI [2])
C0012634 (UMLS CUI-2)
C1457887 (UMLS CUI-3)
C1457887 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C0013516 (UMLS CUI-2)
C1623258 (UMLS CUI [1,2])
C0013516 (UMLS CUI [1,2])
C0013516 (UMLS CUI [1,2])
C0013516 (UMLS CUI [2])
C0428772 (UMLS CUI [1,2])
C0013516 (UMLS CUI [2])
C0521317 (UMLS CUI [1,2])
C0521317 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2])
C0428772 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2])
C0600091 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C0474523 (UMLS CUI [2])
C0600091 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C2347783 (UMLS CUI [2])
C1519795 (UMLS CUI [1,2])