ID
4035
Description
ODM derived from http://clinicaltrials.gov/show/NCT01361334
Link
http://clinicaltrials.gov/show/NCT01361334
Keywords
Versions (6)
- 4/11/13 4/11/13 - Martin Dugas
- 7/26/13 7/26/13 - Martin Dugas
- 4/20/14 4/20/14 - Julian Varghese
- 8/18/15 8/18/15 - Martin Dugas
- 1/14/16 1/14/16 -
- 2/11/16 2/11/16 -
Uploaded on
July 26, 2013
DOI
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License
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT01361334 Acute Myeloid Leukemia
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Description
Patients with a valid option for intensive chemotherapy and/or stem cell transplantation (Patients after allogeneic stem cell transplant must be off immunosuppressive agents for at least 2 weeks prior to study entry and Graft-versus host disease must have resolved to Grade ≤2)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C2349099
- UMLS CUI 2011AA
- C0683525
- UMLS CUI 2011AA
- C0392920
- SNOMED CT 2011_0131
- 150415003
- UMLS CUI 2011AA
- C1504389
- MedDRA 14.1
- 10063581
- UMLS CUI 2011AA
- C0332197
- SNOMED CT 2011_0131
- 2667000
- UMLS CUI 2011AA
- C0021081
- SNOMED CT 2011_0131
- 372823004, 69431002
- UMLS CUI 2011AA
- C0018133
- SNOMED CT 2011_0131
- 234646005
- MedDRA 14.1
- 10018651
- ICD-10-CM Version 2010
- D89.813
- ICD-9-CM Version 2011
- 279.50
- UMLS CUI 2011AA
- C1514893
- UMLS CUI 2011AA
- C0441800
- SNOMED CT 2011_0131
- 258349007
- LOINC Version 232
- MTHU003112
Description
History of cancer that according to the Investigator might confound the assessment of the endpoints of the study
Data type
boolean
Alias
- UMLS CUI 2011AA
- C2735088
- LOINC Version 232
- MTHU034770
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C1516048
- UMLS CUI 2011AA
- C2349179
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
Description
Uncontrolled peptic ulcer disease or clinically significant gastrointestinal abnormalities which interfere with oral dosing or any unstable or serious concurrent condition (e.g., active uncontrolled infection)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0030920
- SNOMED CT 2011_0131
- 13200003
- MedDRA 14.1
- 10034341
- ICD-10-CM Version 2010
- K27
- ICD-9-CM Version 2011
- 533
- UMLS CUI 2011AA
- C0521362
- LOINC Version 232
- MTHU031867
- UMLS CUI 2011AA
- C1704258
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C1527415
- SNOMED CT 2011_0131
- 26643006
- HL7 V3 2006_05
- _OralRoute
- UMLS CUI 2011AA
- C0178602
- SNOMED CT 2011_0131
- 260911001
- UMLS CUI 2011AA
- C0443343
- SNOMED CT 2011_0131
- 263922001
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0021311
- SNOMED CT 2011_0131
- 257551009
- MedDRA 14.1
- 10021789
Description
Poorly controlled hypertension [defined as systolic blood pressure (SBP) of >=140 mmHg or diastolic blood pressure (DBP) of >90 mmHg]. Note: Initiation or adjustment of antihypertensive medication(s) is permitted prior to study entry. BP must be re-assessed on two occasions that are separated by a minimum of 1 hour. on each of these occasions, the mean (of 3 readings) SBP / DBP values from each BP assessment must be <140/90 mmHg in order for a subject to be eligible for the study
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205169
- SNOMED CT 2011_0131
- 556001
- UMLS CUI 2011AA
- C2587213
- SNOMED CT 2011_0131
- 31509003
- UMLS CUI 2011AA
- C0020538
- SNOMED CT 2011_0131
- 38341003
- MedDRA 14.1
- 10020772
- LOINC Version 232
- MTHU020789
- ICD-10-CM Version 2010
- I10
- ICD-9-CM Version 2011
- 997.91
- CTCAE 1105E
- E13785
- UMLS CUI 2011AA
- C1306620
- MedDRA 14.1
- 10005756
- UMLS CUI 2011AA
- C0428883
- SNOMED CT 2011_0131
- 271650006
Description
Prolongation of corrected QT interval (QTc) >480 milliseconds
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1560305
Description
History of any one of more of the following cardiovascular conditions within the past 6 months: cardiac angioplasty or stenting, myocardial infarction, unstable angina, symptomatic peripheral vascular disease, class III or IV congestive heart failure, as defined by the New York Heart Association (NYHA)
Data type
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C1522601
- UMLS CUI 2011AA
- C0162577
- SNOMED CT 2011_0131
- 418285008
- MedDRA 14.1
- 10002475
- LOINC Version 232
- MTHU011020
- UMLS CUI 2011AA
- CL371838
- UMLS CUI 2011AA
- C0027051
- SNOMED CT 2011_0131
- 22298006
- MedDRA 14.1
- 10028596
- LOINC Version 232
- MTHU035551
- ICD-10-CM Version 2010
- I21-I22
- ICD-9-CM Version 2011
- 410
- CTCAE 1105E
- E10152
- UMLS CUI 2011AA
- C0002965
- SNOMED CT 2011_0131
- 4557003
- MedDRA 14.1
- 10002388
- ICD-10-CM Version 2010
- I20.0
- ICD-9-CM Version 2011
- 411.1
- UMLS CUI 2011AA
- C0085096
- SNOMED CT 2011_0131
- 400047006
- MedDRA 14.1
- 10034636
- LOINC Version 232
- MTHU020791
- ICD-10-CM Version 2010
- I73.9
- ICD-9-CM Version 2011
- 443.9
- UMLS CUI 2011AA
- C0018802
- SNOMED CT 2011_0131
- 42343007
- MedDRA 14.1
- 10007559
- LOINC Version 232
- MTHU020787
- ICD-10-CM Version 2010
- I50.9
- ICD-9-CM Version 2011
- 428.0
- UMLS CUI 2011AA
- C1319795
- SNOMED CT 2011_0131
- 420913000
- MedDRA 14.1
- 10064081
- UMLS CUI 2011AA
- C1319796
- SNOMED CT 2011_0131
- 422293003
- MedDRA 14.1
- 10064082
Description
History of cerebrovascular infarction or bleeding, pulmonary embolism, or untreated deep venous thrombosis (DVT) within the past 6 months. Note: Subjects with recent DVT who have been treated with therapeutic anti-coagulant agents for at least 6 weeks are eligible
Data type
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0007785
- SNOMED CT 2011_0131
- 432504007
- MedDRA 14.1
- 10060772
- ICD-10-CM Version 2010
- I63.9
- UMLS CUI 2011AA
- C1880018
- UMLS CUI 2011AA
- C0019080
- SNOMED CT 2011_0131
- 50960005
- MedDRA 14.1
- 10055798
- ICD-10-CM Version 2010
- R58
- ICD-9-CM Version 2011
- 459.0
- UMLS CUI 2011AA
- C0034065
- SNOMED CT 2011_0131
- 59282003
- MedDRA 14.1
- 10037377
- ICD-10-CM Version 2010
- I26
- ICD-9-CM Version 2011
- 415.1
- UMLS CUI 2011AA
- C0332155
- SNOMED CT 2011_0131
- 25265005
- UMLS CUI 2011AA
- C0149871
- SNOMED CT 2011_0131
- 128053003
- MedDRA 14.1
- 10051055
- ICD-10-CM Version 2010
- I82.40
Description
Evidence of serious active bleeding or bleeding diathesis (except for bleeding or petechiae due to AML-related thrombocytopenia which will be treated using platelet transfusions). Also, patients with known endobronchial lesions and/or lesions infiltrating major pulmonary vessels will be excluded from the study due to excess risk of bleeding.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205404
- SNOMED CT 2011_0131
- 42745003
- UMLS CUI 2011AA
- C0019080
- SNOMED CT 2011_0131
- 50960005
- MedDRA 14.1
- 10055798
- ICD-10-CM Version 2010
- R58
- ICD-9-CM Version 2011
- 459.0
- UMLS CUI 2011AA
- C1458140
- SNOMED CT 2011_0131
- 248250000
- MedDRA 14.1
- 10005134
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0019080
- SNOMED CT 2011_0131
- 50960005
- MedDRA 14.1
- 10055798
- ICD-10-CM Version 2010
- R58
- ICD-9-CM Version 2011
- 459.0
- UMLS CUI 2011AA
- C0031256
- SNOMED CT 2011_0131
- 50091001
- MedDRA 14.1
- 10034754
- ICD-10-CM Version 2010
- R23.3
- UMLS CUI 2011AA
- CL420107
- UMLS CUI 2011AA
- C0023467
- SNOMED CT 2011_0131
- 91861009
- MedDRA 14.1
- 10000880
- ICD-10-CM Version 2010
- C92.0
- ICD-9-CM Version 2011
- 205.0
- UMLS CUI 2011AA
- C0699792
- SNOMED CT 2011_0131
- 263498003
- UMLS CUI 2011AA
- C0040034
- SNOMED CT 2011_0131
- 302215000
- MedDRA 14.1
- 10043554
- ICD-10-CM Version 2010
- D69.6
- ICD-9-CM Version 2011
- 287.5
- CTCAE 1105E
- E12207
- UMLS CUI 2011AA
- CL425201
- UMLS CUI 2011AA
- C2985135
- UMLS CUI 2011AA
- C0273454
- SNOMED CT 2011_0131
- 210790008
- MedDRA 14.1
- 10022320
- ICD-10-CM Version 2010
- S25.4
- ICD-9-CM Version 2011
- 901.40
Description
Prior major surgery or trauma within 28 days prior to first dose of study drug
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0679637
- UMLS CUI 2011AA
- C0175677
- SNOMED CT 2011_0131
- 417746004
- MedDRA 14.1
- 10022116
- ICD-10-CM Version 2010
- T14.9
- UMLS CUI 2011AA
- C0439231
- SNOMED CT 2011_0131
- 258706009
- HL7 V3 2006_05
- MO
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
Description
Treatment with an investigational agent within 28 days or 5 half-lives, whichever is longer prior to the first dose of study drug (for bevacizumab 60 days).
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0439231
- SNOMED CT 2011_0131
- 258706009
- HL7 V3 2006_05
- MO
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
- UMLS CUI 2011AA
- C0796392
- SNOMED CT 2011_0131
- 409406007
Description
Concurrent cytoreductive chemotherapy (hydroxyurea must be discontinued at least one day before start of study medication)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205420
- SNOMED CT 2011_0131
- 68405009
- UMLS CUI 2011AA
- C0392920
- SNOMED CT 2011_0131
- 150415003
- UMLS CUI 2011AA
- C0864494
- UMLS CUI 2011AA
- C0020402
- SNOMED CT 2011_0131
- 56602009
Description
Known immediate or delayed hypersensitivity reaction or idiosyncrasy to pazopanib
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0020517
- SNOMED CT 2011_0131
- 418634005
- ICD-10-CM Version 2010
- T78.40
- UMLS CUI 2011AA
- C0231191
- SNOMED CT 2011_0131
- 56840009
- UMLS CUI 2011AA
- C1831796
- SNOMED CT 2011_0131
- 443763005
Description
Patients with psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205486
- SNOMED CT 2011_0131
- 60224009
- UMLS CUI 2011AA
- C0241888
- SNOMED CT 2011_0131
- 255401001
- UMLS CUI 2011AA
- C0037468
- UMLS CUI 2011AA
- C1517526
- UMLS CUI 2011AA
- C0348080
- SNOMED CT 2011_0131
- 260905004
- HL7 V3 2006_05
- COND
- UMLS CUI 2011AA
- CL414898
- UMLS CUI 2011AA
- C0525058
Description
Pregnant or lactating and actively breastfeeding patients
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
Description
Patients taking any of the following prohibited medication:
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1512806
- UMLS CUI 2011AA
- CL407060
- UMLS CUI 2011AA
- C0332282
- SNOMED CT 2011_0131
- 255260001
- UMLS CUI 2011AA
- C0683610
- UMLS CUI 2011AA
- C0013227
Description
clarithromycin, telithromycin, troleandomycin (antibiotics)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0055856
- SNOMED CT 2011_0131
- 83999008
- LOINC Version 232
- MTHU006897
- UMLS CUI 2011AA
- C1452484
- SNOMED CT 2011_0131
- 395260006
- LOINC Version 232
- MTHU016681
- UMLS CUI 2011AA
- C0702222
- SNOMED CT 2011_0131
- 371016002
- LOINC Version 232
- MTHU008495
- UMLS CUI 2011AA
- C0003232
- SNOMED CT 2011_0131
- 255631004
Description
ritonavir, indinavir, saquinavir, nelfinavir, amprenavir, lopinavir (HIV protease inhibitors)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0292818
- SNOMED CT 2011_0131
- 386896009
- LOINC Version 232
- MTHU013855
- UMLS CUI 2011AA
- C0376637
- SNOMED CT 2011_0131
- 108695003
- LOINC Version 232
- MTHU013846
- UMLS CUI 2011AA
- C0286738
- SNOMED CT 2011_0131
- 108700005
- LOINC Version 232
- MTHU008513
- UMLS CUI 2011AA
- C0525005
- SNOMED CT 2011_0131
- 108706004
- LOINC Version 232
- MTHU013848
- UMLS CUI 2011AA
- C0754188
- SNOMED CT 2011_0131
- 116088006
- LOINC Version 232
- MTHU013842
- UMLS CUI 2011AA
- C0674432
- SNOMED CT 2011_0131
- 129475001
- LOINC Version 232
- MTHU014678
- UMLS CUI 2011AA
- C0162714
Description
itraconazole, ketoconazole, voriconazole, fluconazole (antifungals)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0064113
- SNOMED CT 2011_0131
- 387532006
- LOINC Version 232
- MTHU002298
- UMLS CUI 2011AA
- C0022625
- SNOMED CT 2011_0131
- 387216007
- LOINC Version 232
- MTHU002299
- UMLS CUI 2011AA
- C0393080
- SNOMED CT 2011_0131
- 385469007
- LOINC Version 232
- MTHU015011
- UMLS CUI 2011AA
- C0016277
- SNOMED CT 2011_0131
- 31865003
- LOINC Version 232
- MTHU002296
- UMLS CUI 2011AA
- C0003308
- SNOMED CT 2011_0131
- 373219008
Description
nefazodone (antidepressant)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0068485
- SNOMED CT 2011_0131
- 108435006
- LOINC Version 232
- MTHU003461
- UMLS CUI 2011AA
- C0003289
- SNOMED CT 2011_0131
- 372720008
- LOINC Version 232
- MTHU006782
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Eligibility
- StudyEvent: Eligibility
397669002 (SNOMED CT 2011_0131)
55149002 (SNOMED CT 2011_0131)
CL415337 (UMLS CUI 2011AA)
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279.50 (ICD-9-CM Version 2011)
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10028596 (MedDRA 14.1)
MTHU035551 (LOINC Version 232)
I21-I22 (ICD-10-CM Version 2010)
410 (ICD-9-CM Version 2011)
E10152 (CTCAE 1105E)
C0002965 (UMLS CUI 2011AA)
4557003 (SNOMED CT 2011_0131)
10002388 (MedDRA 14.1)
I20.0 (ICD-10-CM Version 2010)
411.1 (ICD-9-CM Version 2011)
C0085096 (UMLS CUI 2011AA)
400047006 (SNOMED CT 2011_0131)
10034636 (MedDRA 14.1)
MTHU020791 (LOINC Version 232)
I73.9 (ICD-10-CM Version 2010)
443.9 (ICD-9-CM Version 2011)
C0018802 (UMLS CUI 2011AA)
42343007 (SNOMED CT 2011_0131)
10007559 (MedDRA 14.1)
MTHU020787 (LOINC Version 232)
I50.9 (ICD-10-CM Version 2010)
428.0 (ICD-9-CM Version 2011)
C1319795 (UMLS CUI 2011AA)
420913000 (SNOMED CT 2011_0131)
10064081 (MedDRA 14.1)
C1319796 (UMLS CUI 2011AA)
422293003 (SNOMED CT 2011_0131)
10064082 (MedDRA 14.1)
392521001 (SNOMED CT 2011_0131)
C0007785 (UMLS CUI 2011AA)
432504007 (SNOMED CT 2011_0131)
10060772 (MedDRA 14.1)
I63.9 (ICD-10-CM Version 2010)
C1880018 (UMLS CUI 2011AA)
C0019080 (UMLS CUI 2011AA)
50960005 (SNOMED CT 2011_0131)
10055798 (MedDRA 14.1)
R58 (ICD-10-CM Version 2010)
459.0 (ICD-9-CM Version 2011)
C0034065 (UMLS CUI 2011AA)
59282003 (SNOMED CT 2011_0131)
10037377 (MedDRA 14.1)
I26 (ICD-10-CM Version 2010)
415.1 (ICD-9-CM Version 2011)
C0332155 (UMLS CUI 2011AA)
25265005 (SNOMED CT 2011_0131)
C0149871 (UMLS CUI 2011AA)
128053003 (SNOMED CT 2011_0131)
10051055 (MedDRA 14.1)
I82.40 (ICD-10-CM Version 2010)
42745003 (SNOMED CT 2011_0131)
C0019080 (UMLS CUI 2011AA)
50960005 (SNOMED CT 2011_0131)
10055798 (MedDRA 14.1)
R58 (ICD-10-CM Version 2010)
459.0 (ICD-9-CM Version 2011)
C1458140 (UMLS CUI 2011AA)
248250000 (SNOMED CT 2011_0131)
10005134 (MedDRA 14.1)
C1554961 (UMLS CUI 2011AA)
E (HL7 V3 2006_05)
C0019080 (UMLS CUI 2011AA)
50960005 (SNOMED CT 2011_0131)
10055798 (MedDRA 14.1)
R58 (ICD-10-CM Version 2010)
459.0 (ICD-9-CM Version 2011)
C0031256 (UMLS CUI 2011AA)
50091001 (SNOMED CT 2011_0131)
10034754 (MedDRA 14.1)
R23.3 (ICD-10-CM Version 2010)
CL420107 (UMLS CUI 2011AA)
C0023467 (UMLS CUI 2011AA)
91861009 (SNOMED CT 2011_0131)
10000880 (MedDRA 14.1)
C92.0 (ICD-10-CM Version 2010)
205.0 (ICD-9-CM Version 2011)
C0699792 (UMLS CUI 2011AA)
263498003 (SNOMED CT 2011_0131)
C0040034 (UMLS CUI 2011AA)
302215000 (SNOMED CT 2011_0131)
10043554 (MedDRA 14.1)
D69.6 (ICD-10-CM Version 2010)
287.5 (ICD-9-CM Version 2011)
E12207 (CTCAE 1105E)
CL425201 (UMLS CUI 2011AA)
C2985135 (UMLS CUI 2011AA)
C0273454 (UMLS CUI 2011AA)
210790008 (SNOMED CT 2011_0131)
10022320 (MedDRA 14.1)
S25.4 (ICD-10-CM Version 2010)
901.40 (ICD-9-CM Version 2011)
C0175677 (UMLS CUI 2011AA)
417746004 (SNOMED CT 2011_0131)
10022116 (MedDRA 14.1)
T14.9 (ICD-10-CM Version 2010)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C2348558 (UMLS CUI 2011AA)
C0013230 (UMLS CUI 2011AA)
C0439231 (UMLS CUI 2011AA)
258706009 (SNOMED CT 2011_0131)
MO (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C2348558 (UMLS CUI 2011AA)
C0796392 (UMLS CUI 2011AA)
409406007 (SNOMED CT 2011_0131)
68405009 (SNOMED CT 2011_0131)
C0392920 (UMLS CUI 2011AA)
150415003 (SNOMED CT 2011_0131)
C0864494 (UMLS CUI 2011AA)
C0020402 (UMLS CUI 2011AA)
56602009 (SNOMED CT 2011_0131)
418634005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0231191 (UMLS CUI 2011AA)
56840009 (SNOMED CT 2011_0131)
C1831796 (UMLS CUI 2011AA)
443763005 (SNOMED CT 2011_0131)
60224009 (SNOMED CT 2011_0131)
C0241888 (UMLS CUI 2011AA)
255401001 (SNOMED CT 2011_0131)
C0037468 (UMLS CUI 2011AA)
C1517526 (UMLS CUI 2011AA)
C0348080 (UMLS CUI 2011AA)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
CL414898 (UMLS CUI 2011AA)
C0525058 (UMLS CUI 2011AA)
10036586 (MedDRA 14.1)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
C0030705 (UMLS CUI 2011AA)
116154003 (SNOMED CT 2011_0131)
CL407060 (UMLS CUI 2011AA)
C0332282 (UMLS CUI 2011AA)
255260001 (SNOMED CT 2011_0131)
C0683610 (UMLS CUI 2011AA)
C0013227 (UMLS CUI 2011AA)
83999008 (SNOMED CT 2011_0131)
MTHU006897 (LOINC Version 232)
C1452484 (UMLS CUI 2011AA)
395260006 (SNOMED CT 2011_0131)
MTHU016681 (LOINC Version 232)
C0702222 (UMLS CUI 2011AA)
371016002 (SNOMED CT 2011_0131)
MTHU008495 (LOINC Version 232)
C0003232 (UMLS CUI 2011AA)
255631004 (SNOMED CT 2011_0131)
386896009 (SNOMED CT 2011_0131)
MTHU013855 (LOINC Version 232)
C0376637 (UMLS CUI 2011AA)
108695003 (SNOMED CT 2011_0131)
MTHU013846 (LOINC Version 232)
C0286738 (UMLS CUI 2011AA)
108700005 (SNOMED CT 2011_0131)
MTHU008513 (LOINC Version 232)
C0525005 (UMLS CUI 2011AA)
108706004 (SNOMED CT 2011_0131)
MTHU013848 (LOINC Version 232)
C0754188 (UMLS CUI 2011AA)
116088006 (SNOMED CT 2011_0131)
MTHU013842 (LOINC Version 232)
C0674432 (UMLS CUI 2011AA)
129475001 (SNOMED CT 2011_0131)
MTHU014678 (LOINC Version 232)
C0162714 (UMLS CUI 2011AA)
387532006 (SNOMED CT 2011_0131)
MTHU002298 (LOINC Version 232)
C0022625 (UMLS CUI 2011AA)
387216007 (SNOMED CT 2011_0131)
MTHU002299 (LOINC Version 232)
C0393080 (UMLS CUI 2011AA)
385469007 (SNOMED CT 2011_0131)
MTHU015011 (LOINC Version 232)
C0016277 (UMLS CUI 2011AA)
31865003 (SNOMED CT 2011_0131)
MTHU002296 (LOINC Version 232)
C0003308 (UMLS CUI 2011AA)
373219008 (SNOMED CT 2011_0131)
108435006 (SNOMED CT 2011_0131)
MTHU003461 (LOINC Version 232)
C0003289 (UMLS CUI 2011AA)
372720008 (SNOMED CT 2011_0131)
MTHU006782 (LOINC Version 232)