ID
43936
Descripción
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
Palabras clave
Versiones (2)
- 29/5/17 29/5/17 -
- 20/9/21 20/9/21 -
Subido en
20 de septiembre de 2021
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
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
Descripción
Pharmacogenetic Research - Tumor - Informed Consent
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C0006826
Descripción
informed consent
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0021430
Descripción
Date informed consent obtained
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0514044
- UMLS CUI [1,2]
- C0011008
Descripción
reason informed consent was not obtained
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1705116
- UMLS CUI [1,3]
- C0392360
Descripción
tumor sample
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0475358
Descripción
Date tumor sample taken
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0475358
Descripción
withdraw consent
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2349954
Descripción
Inclusion Criteria Worksheet
Alias
- UMLS CUI-1
- C1512693
- UMLS CUI-2
- C1516637
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0021430
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0853879
- UMLS CUI [2]
- C0278488
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1515559
- UMLS CUI [1,2]
- C0587081
- UMLS CUI [2]
- C0853879
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0278488
- UMLS CUI [2]
- C0853879
Descripción
Check YES if this is applicable for the subject.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0678222
- UMLS CUI [1,2]
- C0205269
Descripción
Check YES if this is applicable for the subject.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0728747
Descripción
Check YES if this is applicable for the subject, otherwise check NO.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1563119
- UMLS CUI [2]
- C0242656
- UMLS CUI [3]
- C0279025
Descripción
Check YES if this is applicable for the subject
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0686377
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0001779
- UMLS CUI [1,2]
- C0681850
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1520224
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1513041
- UMLS CUI [1,2]
- C1709926
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0003738
- UMLS CUI [1,2]
- C0475358
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0023671
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
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
Descripción
Check YES if this is applicable for the subject
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1522449
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0232174
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0175795
- UMLS CUI [1,2]
- C2712086
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1710477
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0232804
Descripción
Inclusion Criteria check one box for each question: If any INCLUSION CRITERIA question is answered NO, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0221130
- UMLS CUI [2]
- C0232741
Descripción
Exclusion Criteria Worksheet
Alias
- UMLS CUI-1
- C0680251
Descripción
Exclusion Criteria check one box for each question: If any EXCLUSION CRITERIA question is answered YES, this subject must NOT enter this study.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0549206
Descripción
Malabsorption Syndrome, disease significantly affecting gastrointestinal function, resection of the stomach or small bowel, or ulcerative colitis
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0024523
- UMLS CUI [2]
- C0017178
Descripción
history of other malignancy
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0027651
- UMLS CUI [1,2]
- C0262926
Descripción
concurrent disease or condition
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C1548788
Descripción
unresolved or unstable, serious toxicity
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0013221
- UMLS CUI [1,2]
- C0013230
Descripción
active or uncontrolled infection
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0009450
Descripción
dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Descripción
history of uncontrolled or symptomatic angina, arrhythmias, or congestive heart failure
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0018799
Descripción
coumarin-derivative anticoagulants
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0003280
- UMLS CUI [2]
- C0010207
Descripción
history of, or clinical evidence of leptomeningeal carcinomatosis
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0220654
Descripción
concurrent anti-cancer therapy other than capecitabine
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0920425
Descripción
Check NO if this is applicable for the subject
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0012544
Descripción
concurrent treatment with an investigational agent or participating in another clinical trial
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
Descripción
used an investigational drug
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013230
Descripción
immediate or delayed hypersensitivity reaction or idiosyncrasy
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1384663
- UMLS CUI [2,1]
- C0231191
- UMLS CUI [2,2]
- C1384663
Descripción
immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to capecitabine, fluorouracil or any excipients?
Tipo de datos
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
Descripción
dihydropyrimidine dehydrogenase (DPD) deficiency
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1959620
Descripción
Inclusion and Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
- UMLS CUI-2
- C1512693
- UMLS CUI-3
- C1516637
Descripción
Protocol code
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1507394
- UMLS CUI [1,2]
- C0600091
Descripción
Session number
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1883017
- UMLS CUI [1,2]
- C0750480
Descripción
Subject number
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2348585
Descripción
meet all entry criteria
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013893
Descripción
violation of the inclusion criteria
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C1512693
- UMLS CUI [2]
- C1516637
Descripción
violation of the exclusion criteria
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C0680251
- UMLS CUI [2]
- C1516637
Descripción
Current Medical Conditions / Baseline Signs and Symptoms
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0012634
- UMLS CUI-3
- C1457887
Descripción
current medical conditions, baseline signs or symptoms
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1457887
Descripción
If YES, record all screening clinical signs and symptoms below according to the instructions on the facing page.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1457887
Descripción
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
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C3887242
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C1457887
Descripción
Physical Exam (Vital Signs, Weight, Height)
Alias
- UMLS CUI-1
- C0518766
Descripción
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
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0011008
Descripción
Blood pressure systolic
Tipo de datos
integer
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Descripción
Blood pressure diastolic
Tipo de datos
integer
Unidades de medida
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Descripción
Heart rate
Tipo de datos
integer
Unidades de medida
- beats/min
Alias
- UMLS CUI [1]
- C0018810
Descripción
Height
Tipo de datos
integer
Unidades de medida
- cm
Alias
- UMLS CUI [1]
- C0005890
Descripción
Weight
Tipo de datos
float
Unidades de medida
- kg
Alias
- UMLS CUI [1]
- C0005910
Descripción
Temperature
Tipo de datos
float
Unidades de medida
- °C
Alias
- UMLS CUI [1]
- C0005903
Descripción
ECOG Performance Status
Alias
- UMLS CUI-1
- C1520224
Descripción
Cardiac Assessments Screening
Alias
- UMLS CUI-1
- C1623258
- UMLS CUI-2
- C0013516
Descripción
If NO, record details on the INVESTIGATOR COMMENT LOG page. If YES, record details below.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0430456
Descripción
Date of assessment
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1623258
Descripción
ECG results
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1623258
Descripción
If YES, record the abnormality on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page at Screening.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1623258
Descripción
If YES, record details below.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0013516
Descripción
Institution name
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0013516
Descripción
Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0013516
Descripción
Left ventricular ejection fraction
Tipo de datos
integer
Unidades de medida
- %
Alias
- UMLS CUI [1]
- C0428772
- UMLS CUI [2]
- C0013516
Descripción
Lower limit of normal
Tipo de datos
integer
Unidades de medida
- %
Alias
- UMLS CUI [1,1]
- C1518030
- UMLS CUI [1,2]
- C0428772
- UMLS CUI [2]
- C0013516
Descripción
If YES, record details below.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0521317
Descripción
Institution name
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1301943
- UMLS CUI [1,2]
- C0521317
Descripción
Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0521317
Descripción
Left ventricular ejection fraction
Tipo de datos
integer
Unidades de medida
- %
Alias
- UMLS CUI [1]
- C0428772
- UMLS CUI [2]
- C0521317
Descripción
NOTE: If left ventricular ejection fraction is not within institutional range of normal, the subject must not enter the study.
Tipo de datos
integer
Unidades de medida
- %
Alias
- UMLS CUI [1,1]
- C1518030
- UMLS CUI [1,2]
- C0428772
- UMLS CUI [2]
- C0521317
Descripción
Hematology - Local Lab Screening
Alias
- UMLS CUI-1
- C0474523
Descripción
Any clinically significant laboratory abnormalities must be recorded on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0022877
- UMLS CUI [1,2]
- C0600091
Descripción
Lab name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1882331
Descripción
Date hematology sample taken
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [2]
- C0474523
Descripción
Units
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1519795
Descripción
Hemoglobin
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0518015
Descripción
Hematocrit
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0518014
Descripción
RBC
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0014772
Descripción
Platelets
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0032181
Descripción
Total WBC
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0023508
Descripción
Neutrophils
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0948762
Descripción
Granulocytes
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0857490
Descripción
Lymphocytes
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0200635
Descripción
Monocytes
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0200637
Descripción
Eosinophils
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0200638
Descripción
Basophils
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0200641
Descripción
Clinical Chemistry - Local Lab Screening
Alias
- UMLS CUI-1
- C2347783
Descripción
Any clinically significant laboratory abnormalities must be recorded on the CURRENT MEDICAL CONDITIONS / BASELINE SIGNS AND SYMPTOMS page
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0022877
- UMLS CUI [1,2]
- C0600091
Descripción
Lab name
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1882331
Descripción
Date clinical chemistry sample taken
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [2]
- C2347783
Descripción
Sodium
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0337443
Descripción
Potassium
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0202194
Descripción
Chloride
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201952
Descripción
Bicarbonate
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0202059
Descripción
Calcium
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201925
Descripción
Glucose
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0202042
Descripción
Total Protein
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0555903
Descripción
Albumin
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201838
Descripción
Uric acid
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0202239
Descripción
Creatinine
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201976
Descripción
BUN
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0005845
Descripción
Urea
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0523961
Descripción
Total bilirubin
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201913
Descripción
Alkaline phosphatase
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201850
Descripción
AST (SGOT)
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201899
Descripción
ALT (SGPT)
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201836
Descripción
NOTE: Refer to the creatinine clearance worksheet for calculation.
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0373595
Descripción
Creatinine Clearance Worksheet
Tipo de datos
float
Unidades de medida
- kg
Alias
- UMLS CUI [1]
- C0005910
Descripción
Creatinine Clearance Worksheet
Tipo de datos
integer
Unidades de medida
- cm
Alias
- UMLS CUI [1]
- C0005890
Descripción
Creatinine Clearance Worksheet
Tipo de datos
integer
Unidades de medida
- years
Alias
- UMLS CUI [1]
- C0001779
Descripción
Creatinine Clearance Worksheet
Tipo de datos
float
Alias
- UMLS CUI [1]
- C0201976
Descripción
Creatinine Clearance Worksheet
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0201976
- UMLS CUI [1,2]
- C1519795
Similar models
XELODA and Lapatinib Advanced or Metastatic Breast Cancer Screening NCT00078572
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])