Informações:
Falhas:
ID
42617
Descrição
Study ID: 109275 Clinical Study ID: 109275 Study Title: An Open-Label, Single Sequence Study to Examine the Effects of Esomeprazole on the Pharmacokinetics of Orally Administered Lapatinib in Subjects with Metastatic ErbB2 Positive Breast Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Lapatinib, Esomeprazole Trade Name: lapatinib plus esomeprazole Study Indication: Neoplasms, Breast
Palavras-chave
Versões (2)
- 14/06/2020 14/06/2020 -
- 17/09/2021 17/09/2021 -
Titular dos direitos
GlaxoSmithKline
Transferido a
17 de setembro de 2021
DOI
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Licença
Creative Commons BY-NC 4.0
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Effects of Esomeprazole on Lapatinib in Subjects with Breast Cancer; 109275
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- StudyEvent: ODM
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Clinical trial participant (person), Person Initials
Item
Subject initials
text
C1997894 (UMLS CUI [1,1])
C2986440 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
Patient date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Clinical Trial Subject Unique Identifier
Item
Subject number
text
C2348585 (UMLS CUI [1])
Date of visit, Assessment Date
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C2985720 (UMLS CUI [1,2])
Patient date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
CL Item
Male (1)
CL Item
Hispanic or Latino (1)
CL Item
Not Hispanic or Latino (2)
CL Item
African American/African Heritage (1)
CL Item
American Indian or Alaskan Native (2)
CL Item
Asian - Central/South Asian Heritage (3)
CL Item
Asian - East Asian Heritage (4)
CL Item
Asian - Japanese Heritage (5)
CL Item
Asian - South East Asian Heritage (6)
CL Item
Native Hawaiian or Other Pacific Islander (7)
CL Item
White - Arabic/North African Heritage (8)
CL Item
White - White/Caucasian/European Heritage (9)
Eligibility Determination
Item
Did the subject meet all the entry criteria?
boolean
C0013893 (UMLS CUI [1])
Breast Carcinoma, Metastatic to, Estrogen receptor positive breast cancer; Malignant Neoplasms, Unresponsive to Treatment
Item
Histologically or cytologically confirmed diagnosis of: • Metastatic breast cancer that overexpresses ErbB2 (3+ by IHC, FISH, or CISH positive) OR • Recurrent, advanced, or metastatic solid tumor malignancy that is refractory to standard therapies, for which there is no approved therapy, and for which lapatinib in combination with one of the permitted anti-cancer regimens in the companion rollover protocol (EGF111767) may be suitable.
boolean
C0678222 (UMLS CUI [1,1])
C0036525 (UMLS CUI [1,2])
C2938924 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
C0036525 (UMLS CUI [1,2])
C2938924 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
Age
Item
Is at least 18 years of age and not greater than 75 years of age.
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Is male or female.
boolean
C0079399 (UMLS CUI [1])
Childbearing Potential
Item
A female is eligible to enter and participate in the study if she is of: a. Non-childbearing potential (i.e. physiologically incapable of becoming pregnant), including any female who: • Has had a hysterectomy • Has had a bilateral oophorectomy (ovariectomy) • Has had a bilateral tubal ligation, or • Is post-menopausal (a demonstration of total cessation of menses for ≥ 1 year) or b. Childbearing potential, has a negative serum pregnancy test at Screening and agrees to one of the following:• Double-barrier contraception (condom with spermicidal jelly, foam, suppository, or film; diaphragm with spermicide; or male condom and diaphragm). • Complete abstinence from sexual intercourse from two weeks prior to administration of the study drug, throughout the active study treatment period, and two weeks post last administration of the study drug. • Vasectomized partner who is sterile prior to the female subject’s entry and is the sole sexual partner for that female.
boolean
C3831118 (UMLS CUI [1])
Oral medication, Able to swallow; Oral medication, Ability, Retained
Item
Is able to swallow and retain oral medication.
boolean
C0175795 (UMLS CUI [1,1])
C2712086 (UMLS CUI [1,2])
C0175795 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0333118 (UMLS CUI [2,3])
C2712086 (UMLS CUI [1,2])
C0175795 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0333118 (UMLS CUI [2,3])
ECOG Performance status
Item
ECOG performance status 0 to 2.
boolean
C1520224 (UMLS CUI [1])
Bone Marrow, physiological aspects
Item
Adequate bone marrow function. • Hemoglobin ≥ 9 gm/dL (90g/L). • Absolute granulocyte count ≥ 1,500/mm3 (1.5 x 109/L). • Platelets ≥ 75,000/mm3 (75 x 109/L).
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0031843 (UMLS CUI [1,2])
Estimation of creatinine clearance by Cockcroft-Gault formula
Item
Calculated creatinine clearance (CrCl) ≥ 50 ml/min based on Cockcroft and Gault
boolean
C2711451 (UMLS CUI [1])
Bilirubin, total measurement
Item
Total bilirubin ≤ 1.5 X upper limit of normal of institutional values.
boolean
C0201913 (UMLS CUI [1])
Alanine aminotransferase measurement
Item
Alanine transaminase (ALT) ≤ 3 times the upper limit of the institutional values or ≤ 5 times ULN with documented liver metastases
boolean
C0201836 (UMLS CUI [1])
Left ventricular ejection fraction
Item
Has a left ventricular ejection fraction (LVEF) within the normal institutional range based on ECHO or MUGA.
boolean
C0428772 (UMLS CUI [1])
Life Expectancy
Item
Life expectancy of ≥ 12 weeks
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
boolean
C0021430 (UMLS CUI [1])
Pregnancy; Breast Feeding
Item
Is pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Malabsorption Syndrome; Disease, Affecting, gastrointestinal function; Colon resection; Stomach, Excision; Small intestine excision
Item
Has malabsorption syndrome, a disease affecting gastrointestinal function, or resection of the colon, stomach or small bowel.
boolean
C0024523 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0516983 (UMLS CUI [2,3])
C4069040 (UMLS CUI [3])
C0161898 (UMLS CUI [4,1])
C0728940 (UMLS CUI [4,2])
C0192601 (UMLS CUI [5])
C0012634 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0516983 (UMLS CUI [2,3])
C4069040 (UMLS CUI [3])
C0161898 (UMLS CUI [4,1])
C0728940 (UMLS CUI [4,2])
C0192601 (UMLS CUI [5])
Liver diseases; Biliary System Disorder
Item
Has current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment)
boolean
C0023895 (UMLS CUI [1])
C3275124 (UMLS CUI [2])
C3275124 (UMLS CUI [2])
Metastatic malignant neoplasm to brain; Leptomeningeal Neoplasms
Item
Has evidence of symptomatic or uncontrolled brain metastases or leptomeningeal disease. Subjects with brain metastases treated by surgery and/or radiotherapy are eligible if neurologically stable and do not require steroids or anticonvulsants for at least 28 days prior to the first dose of study drug.
boolean
C0220650 (UMLS CUI [1])
C0751297 (UMLS CUI [2])
C0751297 (UMLS CUI [2])
Medically unfit, Clinical Trials
Item
Is considered medically unfit for the study by the investigator as a result of the medical interview, physical exam, or screening investigations.
boolean
C3841806 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,2])
Benzimidazole derivatives, antinematodal, Hypersensitivity; Experimental drug, Idiosyncrasy
Item
Has a known immediate or delayed benzimidazole hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product such as gefitinib [Iressa] and erlotinib [Tarceva].
boolean
C3653457 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0304229 (UMLS CUI [2,1])
C0231191 (UMLS CUI [2,2])
C0020517 (UMLS CUI [1,2])
C0304229 (UMLS CUI [2,1])
C0231191 (UMLS CUI [2,2])
Esomeprazole, Hypersensitivity
Item
Has a known hypersensitivity to esomeprazole.
boolean
C0937846 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0020517 (UMLS CUI [1,2])
Experimental drug, Previous
Item
Has received treatment with any investigational drug in the previous four weeks. (with the exception of lapatinib).
boolean
C0304229 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,2])
Chemotherapy Regimen, Cancer treatment, Previous; Immunotherapy, Cancer treatment, Previous; Biological treatment, Cancer treatment, Previous; Hormone Therapy, Cancer treatment, Previous
Item
Has received chemotherapy, immunotherapy, biologic therapy or hormonal therapy for the treatment of cancer within the past 14 days, with the exception of mitomycin C which is restricted for the past six weeks, and lapatinib. Subjects receiving lapatinib prior to study entry are eligible to participate in the study. NOTE: Any ongoing potentially reversible toxicity from prior anti-cancer therapy that is > Grade 1 or any toxicity from prior anti-cancer therapy that is progressing in severity will render the subject ineligible.
boolean
C0392920 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0021083 (UMLS CUI [2,1])
C0920425 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C1531518 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0205156 (UMLS CUI [3,3])
C0279025 (UMLS CUI [4,1])
C0920425 (UMLS CUI [4,2])
C0205156 (UMLS CUI [4,3])
C0920425 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0021083 (UMLS CUI [2,1])
C0920425 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C1531518 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0205156 (UMLS CUI [3,3])
C0279025 (UMLS CUI [4,1])
C0920425 (UMLS CUI [4,2])
C0205156 (UMLS CUI [4,3])
Pharmaceutical Preparations, prohibition
Item
Is receiving any prohibited medication within the timeframe indicated on the prohibited medication list
boolean
C0013227 (UMLS CUI [1,1])
C0683610 (UMLS CUI [1,2])
C0683610 (UMLS CUI [1,2])
Protocol compliance, Unpermitted
Item
Has physiological, familial, sociological, or geographical conditions that do not permit compliance with the protocol.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
venous access, Inadequate (qualifier)
Item
Has inadequate venous access for protocol-related blood draws.
boolean
C0750164 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
C0205412 (UMLS CUI [1,2])
ECG abnormality
Item
Clinically significant electrocardiogram (ECG) abnormality including baseline QTc prolongation >480msec, 2nd degree (type II), or 3rd degree AV block.
boolean
C0522055 (UMLS CUI [1])
Heparin, Hypersensitivity; Heparin-induced Thrombocytopenia
Item
History of sensitivity to heparin or heparin-induced thrombocytopenia.
boolean
C0019134 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0272285 (UMLS CUI [2])
C0020517 (UMLS CUI [1,2])
C0272285 (UMLS CUI [2])
Red wine; Citrus aurantium; Grapefruit (food); GRAPEFRUIT JUICE
Item
Consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or kumquats, pummelos, exotic citrus fruit (i.e. star fruit, bitter melon), grapefruit hybrids or fruit juices from seven days prior to the first dose of study medication.
boolean
C0349371 (UMLS CUI [1])
C0330922 (UMLS CUI [2])
C0995150 (UMLS CUI [3])
C0452456 (UMLS CUI [4])
C0330922 (UMLS CUI [2])
C0995150 (UMLS CUI [3])
C0452456 (UMLS CUI [4])
Item Group
ECHO/MUGA
C0013516 (UMLS CUI-1)
C0521317 (UMLS CUI-2)
C0521317 (UMLS CUI-2)
Item
Scan Type
text
C0013516 (UMLS CUI [1])
C0521317 (UMLS CUI [2])
C0521317 (UMLS CUI [2])
CL Item
ECHO (1)
CL Item
MUGA (2)
Echocardiography, Date in time, Time; Multiple gated acquisition scanning, Date in time, Time
Item
Date and time of scan
datetime
C0013516 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0521317 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0521317 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
Left ventricular ejection fraction
Item
Left ventricular ejection fraction (LVEF)
integer
C0428772 (UMLS CUI [1])
Item
Scan results
text
C0013516 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
CL Item
Normal (1)
CL Item
Abnormal, describe abnormality (2)
Item
Describe abnormality
text
C0013516 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
C1274040 (UMLS CUI [1,2])
C0521317 (UMLS CUI [2,1])
C1274040 (UMLS CUI [2,2])
Code List
Describe abnormality
Disease
Item
Does the subject have any current or past cancer or non-cancer related medical conditions?
boolean
C0012634 (UMLS CUI [1])
Disease, Sequence Number
Item
Sequence Number
integer
C0012634 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
Disease
Item
Specific Condition
text
C0012634 (UMLS CUI [1])
Disease, Medical Dictionary for Regulatory Activities Terminology (MedDRA), Synonym
Item
MedDRA Synonym
text
C0012634 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
C1140263 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
Item
MedDRA lower level term code
text
C0012634 (UMLS CUI [1,1])
C3898442 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
Code List
MedDRA lower level term code
Disease, Code, Failed
Item
Failed coding
text
C0012634 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
CL Item
Current (1)
CL Item
Past (2)
Item
Tumour Classification at Initial Diagnosis
text
C0677930 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
Code List
Tumour Classification at Initial Diagnosis
CL Item
Cutaneous (1)
CL Item
Non-cutaneous (2)
CL Item
Inflammatory (3)
CL Item
Unknown (4)
CL Item
Other, specify (5)
Malignant Neoplasms, Diagnosis, Date in time
Item
Date of Initial Diagnosis
date
C0006826 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Stage at Initial Diagnosis
text
C0006826 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
C1300072 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
CL Item
0 (1)
CL Item
Ia (2)
CL Item
Ib (3)
CL Item
Ic (4)
CL Item
IIa (5)
CL Item
IIb (6)
CL Item
IIc (7)
CL Item
IIIa (8)
CL Item
IIIb (9)
CL Item
IIIc (10)
CL Item
IVa (11)
CL Item
IVb (12)
CL Item
IVc (13)
CL Item
Unknown (14)
Item
Histology at Initial Diagnosis
text
C0006826 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
CL Item
Adenocarcinoma (1)
CL Item
Infiltrating ductal NOS (2)
CL Item
Lobular invasive (3)
CL Item
Malignant mucinous tumours (4)
CL Item
Squamous (5)
CL Item
Undifferentiated adenocarcinoma (6)
CL Item
Undifferentiated carcinoma (7)
CL Item
Tubular (8)
CL Item
Unknown (9)
CL Item
Other, specify (10)
Item
Other, specify
text
C0006826 (UMLS CUI [1,1])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
C0019638 (UMLS CUI [1,2])
C4071762 (UMLS CUI [1,3])
Item
ErbB2 (Her2/neu) Status ImmunoHisto-Chemistry (IHC)
text
C0006826 (UMLS CUI [1,1])
C1512413 (UMLS CUI [1,2])
C0021044 (UMLS CUI [1,3])
C1512413 (UMLS CUI [1,2])
C0021044 (UMLS CUI [1,3])
Code List
ErbB2 (Her2/neu) Status ImmunoHisto-Chemistry (IHC)
CL Item
1+ (1)
CL Item
2+ (2)
CL Item
3+ (3)
Item
Fluorescence in situ Hybridization (FISH)
text
C0006826 (UMLS CUI [1,1])
C0162789 (UMLS CUI [1,2])
C0162789 (UMLS CUI [1,2])
Code List
Fluorescence in situ Hybridization (FISH)
CL Item
Positive (1)
CL Item
Negative (2)
Neoplasm Metastatis, Date of Diagnosis
Item
Date Metastatic Disease was First Diagnosed
date
C0027627 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,2])
Item
Abdomen/Abdominal Wall
text
C0027627 (UMLS CUI [1,1])
C0000726 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2,1])
C0836916 (UMLS CUI [2,2])
C0000726 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2,1])
C0836916 (UMLS CUI [2,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Adrenals
text
C0027627 (UMLS CUI [1,1])
C0001625 (UMLS CUI [1,2])
C0001625 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bladder
text
C0027627 (UMLS CUI [1,1])
C0005682 (UMLS CUI [1,2])
C0005682 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bone
text
C0027627 (UMLS CUI [1,1])
C0262950 (UMLS CUI [1,2])
C0262950 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Bone Marrow
text
C0027627 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
C0005953 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Cervix
text
C0027627 (UMLS CUI [1,1])
C0007874 (UMLS CUI [1,2])
C0007874 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Chest Wall
text
C0027627 (UMLS CUI [1,1])
C0205076 (UMLS CUI [1,2])
C0205076 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
CNS
text
C0027627 (UMLS CUI [1,1])
C0686377 (UMLS CUI [1,2])
C0686377 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Colon
text
C0027627 (UMLS CUI [1,1])
C0009368 (UMLS CUI [1,2])
C0009368 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Esophagus/Oesophagus
text
C0027627 (UMLS CUI [1,1])
C0014876 (UMLS CUI [1,2])
C0014876 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Head and Neck
text
C0027627 (UMLS CUI [1,1])
C0460004 (UMLS CUI [1,2])
C0460004 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Lymph Nodes
text
C0027627 (UMLS CUI [1,1])
C0024204 (UMLS CUI [1,2])
C0024204 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Oral cavity
text
C0027627 (UMLS CUI [1,1])
C0226896 (UMLS CUI [1,2])
C0226896 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Pancreas
text
C0027627 (UMLS CUI [1,1])
C0030274 (UMLS CUI [1,2])
C0030274 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Peritoneum
text
C0027627 (UMLS CUI [1,1])
C0031153 (UMLS CUI [1,2])
C0031153 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Small Intestine
text
C0027627 (UMLS CUI [1,1])
C0021852 (UMLS CUI [1,2])
C0021852 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
Item
Thyroid
text
C0027627 (UMLS CUI [1,1])
C0040132 (UMLS CUI [1,2])
C0040132 (UMLS CUI [1,2])
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Assessed (3)
CL Item
Not Assessed (1)
CL Item
No (2)
CL Item
Yes, please specify (3)
Neoplasm Metastasis, Other
Item
Please specify
text
C0027627 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
Item Group
Prior Anti-Cancer Therapy
C0920425 (UMLS CUI-1)
C1514463 (UMLS CUI-2)
C1514463 (UMLS CUI-2)
Cancer treatment, Prior Therapy
Item
Has the subject taken any prior cancer related therapy?
boolean
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,2])
Cancer treatment, Prior Therapy, Sequence Number
Item
Sequence Number
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Medication name
Item
Drug Name
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Reported term
Item
Modified reported term
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2826302 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C2826302 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Synonym
Item
GSK Drug synonym
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, Collection, Code
Item
GSK Drug Collection code
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
C1514463 (UMLS CUI [1,2])
C1516698 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
Cancer treatment, Prior Therapy, Code, Failed
Item
Failed coding
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,4])
C1514463 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,4])
Item
Therapy Type
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
CL Item
Biologic Therapy (antibodies, cytokines, vaccines) (1)
CL Item
Chemotherapy (cytotoxics, non-cytotoxics) (2)
CL Item
Hormonal Therapy (3)
CL Item
Immunotherapy (4)
Item
Number of Cycles
integer
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1511572 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
C1514463 (UMLS CUI [1,2])
C1511572 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
Item
Intent
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
CL Item
Neo-adjuvant (1)
CL Item
Adjuvant (2)
CL Item
Advanced or Metastatic (3)
CL Item
Local/Regional (4)
CL Item
Prophylactic (5)
CL Item
Radiosensitizer (6)
CL Item
Maintenance (7)
CL Item
ot Applicable (8)
Cancer treatment, Prior Therapy, Start Date
Item
Start Date
date
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Cancer treatment, Prior Therapy, End Date
Item
Stop Date
date
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Item
Best Response
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
C1514463 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
CL Item
Complete Response (1)
CL Item
Partial Response (2)
CL Item
Stable Disease (3)
CL Item
Progressive Disease (4)
CL Item
Unknown (5)
CL Item
Not Applicable (6)
Item
Cancer therapy treatment
text
C0920425 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,2])
CL Item
Prior Treatment (1)
CL Item
On-Treatment (2)
CL Item
Post-Treatment (3)
Item Group
Anti-Cancer Radiotherapy
C1522449 (UMLS CUI-1)
C0920425 (UMLS CUI-2)
C0920425 (UMLS CUI-2)
Therapeutic radiology procedure, cancer treatment
Item
Has the subject received any prior anti-cancer radiotherapy?
boolean
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,2])
Therapeutic radiology procedure, cancer treatment, Sequence Number
Item
Sequence Number
integer
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Anatomic Site
Item
Site
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, Cumulative Dose
Item
Cumulative Dose
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,3])
Item
Units
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
CL Item
Grays (1)
CL Item
Centigrays (2)
CL Item
x100 Rads (3)
Item
Intent
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
CL Item
Neo-adjuvant (1)
CL Item
Adjuvant (2)
CL Item
Advanced or Metastatic (3)
CL Item
Local/Regional (4)
CL Item
Prophylactic (5)
CL Item
Other (6)
Therapeutic radiology procedure, cancer treatment, Start Date
Item
Start Date
date
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Therapeutic radiology procedure, cancer treatment, End Date
Item
Stop Date
date
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
Item
Best Response
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C2986560 (UMLS CUI [1,3])
CL Item
Complete Response (1)
CL Item
Partial Response (2)
CL Item
Stable Disease (3)
CL Item
Progressive Disease (4)
CL Item
Unknown (5)
CL Item
Not Applicable (6)
Item
Cancer therapy treatment
text
C1522449 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,2])
Code List
Cancer therapy treatment
CL Item
Prior Treatment (1)
CL Item
On Treatment (2)
CL Item
Post Treatment (3)
Vital signs, Date in time, Time
Item
Actual date/time
datetime
C0518766 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Body Height
Item
Height
integer
C0005890 (UMLS CUI [1])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Body mass index
Item
BMI
float
C1305855 (UMLS CUI [1])
heart rate while sitting
Item
Sitting heart rate
integer
C2029904 (UMLS CUI [1])
Systolic Pressure, Sitting position
Item
Sitting blood pressure measurement - Systolic
integer
C0871470 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
C0277814 (UMLS CUI [1,2])
Diastolic blood pressure, Sitting position
Item
Sitting blood pressure measurement - Diastolic
integer
C0428883 (UMLS CUI [1,1])
C0277814 (UMLS CUI [1,2])
C0277814 (UMLS CUI [1,2])
12 lead ECG, Date in time, Time
Item
Date and Time of ECG
datetime
C0430456 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
12 lead ECG, Heart rate
Item
Heart rate
integer
C0430456 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
C0018810 (UMLS CUI [1,2])
12 lead ECG, Electrocardiogram: P-R interval
Item
PR Interval
integer
C0430456 (UMLS CUI [1,1])
C0429087 (UMLS CUI [1,2])
C0429087 (UMLS CUI [1,2])
12 lead ECG, QRS complex duration
Item
QRS Duration
integer
C0430456 (UMLS CUI [1,1])
C0429025 (UMLS CUI [1,2])
C0429025 (UMLS CUI [1,2])
12 lead ECG, QT interval - finding
Item
Uncorrected QT Interval
integer
C0430456 (UMLS CUI [1,1])
C1287082 (UMLS CUI [1,2])
C1287082 (UMLS CUI [1,2])
Item
QTc Interval
integer
C0430456 (UMLS CUI [1,1])
C0855331 (UMLS CUI [1,2])
C0855331 (UMLS CUI [1,2])
CL Item
Normal (1)
CL Item
Abnormal - Not clinically significant (2)
CL Item
Abnormal - Clinically significant (3)
CL Item
No result (not available) (4)
Item Group
12-Lead ECG Abnormalities
C0430456 (UMLS CUI-1)
C1704258 (UMLS CUI-2)
C1704258 (UMLS CUI-2)
12 lead ECG, Abnormality, Date in time, Time
Item
Date and Time of ECG
datetime
C0430456 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C1704258 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Record clinically significant abnormalities
text
C0430456 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,2])
CL Item
No abnormalities (1)
CL Item
Sinus bradycardia (50-59 beats/min) (2)
CL Item
Sinus bradycardia (40-49 beats/min) (3)
CL Item
Sinus bradycardia (30-39 beats/min) (4)
CL Item
Sinus bradycardia (<30 beats/min) (5)
CL Item
Sinus pause (6)
CL Item
Sinus tachycardia (>100 beats/min) (7)
CL Item
Ectopic supraventricular beats (8)
CL Item
Ectopic supraventricular rhythm (9)
CL Item
Wandering atrial pacemaker (10)
CL Item
Multifocal atrial tachycardia (wandering atrial pacemaker w/rate >100 beats/min) (11)
CL Item
Non-sustained supraventricular tachycardia (>100 beats/min, 3-30 beats) (12)
CL Item
Sustained supraventricular tachycardia (>100 beats/min, >30 beats) (13)
CL Item
Atrial flutter (14)
CL Item
Atrial fibrillation (15)
CL Item
Junctional rhythm (<=100 beats/min, defined by narrow QRS complex) (16)
CL Item
Junctional tachycardia (>100 beats/min) (17)
CL Item
Ventricular premature deplorisation (18)
CL Item
Ventricular couplets (19)
CL Item
Bigeminy (20)
CL Item
Trigeminy (21)
CL Item
Electrical alternans (22)
CL Item
R on T phenomenon (23)
CL Item
Ventricular fibrillation (24)
CL Item
Idioventricular rhythm (<=100 beats/min, defined by wide QRS complex) (25)
CL Item
Non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (26)
CL Item
Sustained ventricular tachycardia (>100 beats/min, >30 beats) (27)
CL Item
Wide QRS tachycardia (diagnosis unknown (28)
CL Item
Monomorphic non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (29)
CL Item
Monomorphic sustained ventricular tachycardia (>100 beats/min, >30 beats) (30)
CL Item
Polymorphic non-sustained ventricular tachycardia (>100 beats/min, 3-30 beats) (31)
CL Item
Polymorphic sustained ventricular tachycardia (>100 beats/min, >30 beats) (32)
CL Item
Torsades de Pointes (TdP) (33)
CL Item
Pacemaker (34)
CL Item
First degree AV block (PR interval >200msec) (35)
CL Item
Short PR Intervak (36)
CL Item
Second degree AV block (Mobitz type 1) (37)
CL Item
Second degree AV block (Mobitz type 2) (38)
CL Item
2:1 AV block (39)
CL Item
Third degree AV block (40)
CL Item
Left axis deviation (QRS axis more negative than -30 degrees) (41)
CL Item
Right axis deviation (QRS axis more positive than +100 degrees) (42)
CL Item
Incomplete left bundle branch block (43)
CL Item
Incomplete left bundle branch block (44)
CL Item
Right bundle branch block (45)
CL Item
Left anterior hemiblock (46)
CL Item
Left posterior hemiblock (47)
CL Item
Left bundle branch block (48)
CL Item
Bifascicular block (49)
CL Item
Non-specific intraventricular conduction delay (QRS >=120 msec) (50)
CL Item
Accessory pathway (Wolff-Parkinson-White, Lown-Ganong-Levine (51)
CL Item
QTc prolongation >=500 msec (52)
CL Item
AV dissociation (53)
CL Item
Myocardial infarction, old (54)
CL Item
Myocardial infarction, non Q-wave (55)
CL Item
Non-specific ST-T changes (56)
CL Item
J point elevation (57)
CL Item
ST elevation (58)
CL Item
ST depression (59)
CL Item
ST segment abnormality (60)
CL Item
U waves (61)
CL Item
T wave inversion (62)
CL Item
T wave peaked (63)
CL Item
T waves biphasic (64)
CL Item
T waves flat (65)
CL Item
66)Notched T-waves (66)Notched T-waves)
CL Item
Low QRS voltage (67)
CL Item
T wave abnormality (68)
CL Item
Other abnormal rhythm (69)
CL Item
Other morphology (70)
CL Item
Other conduction (71)
CL Item
Other myocardial infarction (72)
CL Item
Other depolarization/repolarisation (73)
CL Item
Other abnormality/Cardiologist comments (74)
Randomisation
Item
Was the subject able to be randomized?
boolean
C0034656 (UMLS CUI [1])
Randomisation, Numbers
Item
Yes, provide Randomization number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
Randomization, Date in time
Item
Yes, provide Date of randomization
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Item Group
Local Laboratory - Clinical Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
C0008000 (UMLS CUI-2)
Chemistry, Clinical, Laboratory
Item
Laboratory Used For This Sample
date
C0008000 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,2])
Chemistry, Clinical, Reference lab test reference range, Gender
Item
Gender used to determine lab normals
text
C0008000 (UMLS CUI [1,1])
C0883335 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
C0883335 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
Chemistry, Clinical, Reference lab test reference range, Patient date of birth
Item
Date of birth used to determine lab normals
date
C0008000 (UMLS CUI [1,1])
C0883335 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
C0883335 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
Chemistry, Clinical, Laboratory
Item
Laboratory Used For This Sample
date
C0008000 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,2])
Chemistry, Clinical, Sampling, Date in time
Item
Date sample taken
date
C0008000 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Chemistry, Clinical, Fasting
Item
Was the subject fasting for this laboratory?
boolean
C0008000 (UMLS CUI [1,1])
C0015663 (UMLS CUI [1,2])
C0015663 (UMLS CUI [1,2])
Item
Albumin
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C0201838 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Albumin measurement, Result
Item
Albumin - Result
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Albumin measurement, Result, Unit of Measure
Item
Albumin - Units
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Lower limit of reference range
Item
Albumin - Low
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Upper Limit of Normal
Item
Albumin - High
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Albumin measurement, Result, Toxicity Grade
Item
Albumin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201838 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Alkaline Phosphatase
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C0201850 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Alkaline phosphatase measurement, Result
Item
Alkaline Phosphatase - Result
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Unit of Measure
Item
Alkaline Phosphatase - Units
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Lower limit of reference range
Item
Alkaline Phosphatase - Low
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Upper Limit of Normal
Item
Alkaline Phosphatase - High
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Alkaline phosphatase measurement, Result, Toxicity Grade
Item
Alkaline Phosphatase - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201850 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
ALT
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C0201836 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Alanine aminotransferase measurement, Result
Item
ALT - Result
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Unit of Measure
Item
ALT - Units
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Lower limit of reference range
Item
ALT - Low
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Upper Limit of Normal
Item
ALT - High
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Alanine aminotransferase measurement, Result, Toxicity Grade
Item
ALT - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201836 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
AST
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C0201899 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Aspartate aminotransferase measurement, Result
Item
AST - Result
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Unit of Measure
Item
AST - Units
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Lower limit of reference range
Item
AST - Low
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Upper Limit of Normal
Item
AST - High
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Aspartate aminotransferase measurement, Result, Toxicity Grade
Item
AST - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201899 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Direct Bilirubin
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C0201916 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Bilirubin, direct measurement, Result
Item
Direct Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Unit of Measure
Item
Direct Bilirubin - Units
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Lower limit of reference range
Item
Direct Bilirubin - Low
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Upper Limit of Normal
Item
Direct Bilirubin - High
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, direct measurement, Result, Toxicity Grade
Item
Direct Bilirubin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201916 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Total Bilirubin
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C0201913 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Bilirubin, total measurement, Result
Item
Total Bilirubin - Result
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Bilirubin, total measurement, Result, Unit of Measure
Item
Total Bilirubin - Units
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Lower limit of reference range
Item
Total Bilirubin - Low
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Upper Limit of Normal
Item
Total Bilirubin - High
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Bilirubin, total measurement, Result, Toxicity Grade
Item
Total Bilirubin - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201913 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Carbon Dioxide
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C0007012 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Carbon Dioxide, Result
Item
Carbon Dioxide - Result
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Carbon Dioxide, Result, Unit of Measure
Item
Carbon Dioxide - Units
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Lower limit of reference range
Item
Carbon Dioxide - Low
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Upper Limit of Normal
Item
Carbon Dioxide - High
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Carbon Dioxide, Result, Toxicity Grade
Item
Carbon Dioxide - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0007012 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
BUN
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C0005845 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Blood urea nitrogen measurement, Result
Item
BUN - Result
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Unit of Measure
Item
BUN - Units
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Lower limit of reference range
Item
BUN - Low
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Upper Limit of Normal
Item
BUN - High
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Blood urea nitrogen measurement, Result, Toxicity Grade
Item
BUN - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0005845 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Calcium
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C0201925 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Chemistry, Clinical, Calcium measurement, Result
Item
Calcium - Result
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Calcium measurement, Result, Unit of Measure
Item
Calcium - Units
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Lower limit of reference range
Item
Calcium - Low
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Upper Limit of Normal
Item
Calcium - High
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Calcium measurement, Result, Toxicity Grade
Item
Calcium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201925 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Creatinine
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C0201975 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Creatinine measurement, Result
Item
Creatinine - Result
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Creatinine measurement, Result, Unit of Measure
Item
Creatinine - Units
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Lower limit of reference range
Item
Creatinine - Low
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Upper Limit of Normal
Item
Creatinine - High
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine measurement, Result, Toxicity Grade
Item
Creatinine - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0201975 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Magnesium
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C0373675 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Item
Magnesium - Result
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Magnesium measurement, Result, Unit of Measure
Item
Magnesium - Units
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Item
Magnesium - Low
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Item
Magnesium - High
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Magnesium measurement, Result, Toxicity Grade
Item
Magnesium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0373675 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Potassium
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C0202194 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Potassium measurement, Result
Item
Potassium - Result
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Potassium measurement, Result, Unit of Measure
Item
Potassium - Units
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Lower limit of reference range
Item
Potassium - Low
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Upper Limit of Normal
Item
Potassium - High
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Potassium measurement, Result, Toxicity Grade
Item
Potassium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0202194 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Sodium
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C0337443 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Sodium measurement, Result
Item
Sodium - Result
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Sodium measurement, Result, Unit of Measure
Item
Sodium - Units
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Lower limit of reference range
Item
Sodium - Low
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Upper Limit of Normal
Item
Sodium - High
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Sodium measurement, Result, Toxicity Grade
Item
Sodium - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0337443 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
H. pylori serology (IgG)
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C0079488 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Helicobacter pylori, Result
Item
H. pylori serology (IgG) - Result
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Helicobacter pylori, Result, Unit of Measure
Item
H. pylori serology (IgG) - Units
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Lower limit of reference range
Item
H. pylori serology (IgG) - Low
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Upper Limit of Normal
Item
H. pylori serology (IgG) - High
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Helicobacter pylori, Result, Toxicity Grade
Item
H. pylori serology (IgG) - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0079488 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Creatinine Clearance
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C0373595 (UMLS CUI [1,2])
CL Item
No results (1)
CL Item
Results (2)
Chemistry, Clinical, Creatinine clearance measurement, Result
Item
Creatinine Clearance - Result
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Chemistry, Clinical, Creatinine clearance measurement, Result, Unit of Measure
Item
Creatinine Clearance - Units
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Lower limit of reference range
Item
Creatinine Clearance - Low
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Upper Limit of Normal
Item
Creatinine Clearance - High
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Chemistry, Clinical, Creatinine clearance measurement, Result, Toxicity Grade
Item
Creatinine Clearance - Tox Grade
text
C0008000 (UMLS CUI [1,1])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0373595 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Laboratory Procedures, Chemistry, Clinical, Laboratory, Other
Item
Was any test on this page performed at a different lab than specified on this page?
text
C0022885 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0008000 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Item Group
Local Laboratory - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
C0474523 (UMLS CUI-2)
Laboratory, Hematology finding
Item
Laboratory Used For This Sample
text
C0022877 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,2])
Laboratory Procedures, Hematology finding, Gender
Item
Gender used to determine lab normals
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C0079399 (UMLS CUI [1,3])
Laboratory Procedures, Hematology finding, Patient date of birth
Item
Date of birth used to determine lab normals
date
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C0421451 (UMLS CUI [1,3])
Laboratory Procedures, Hematology finding, Sampling, Date in time
Item
Date sample taken
date
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item
RBC
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C0014772 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Red Blood Cell Count measurement, Result
Item
RBC - Result
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Red Blood Cell Count measurement, Result, Unit of Measure
Item
RBC - Units
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Lower limit of reference range
Item
RBC - Low
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Upper Limit of Normal
Item
RBC - High
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Red Blood Cell Count measurement, Result, Toxicity Grade
Item
RBC - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0014772 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Haemoglobin
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Hemoglobin, Result
Item
Haemoglobin - Result
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Hemoglobin, Result, Unit of Measure
Item
Haemoglobin - Units
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Lower limit of reference range
Item
Haemoglobin - Low
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Upper Limit of Normal
Item
Haemoglobin - High
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Hemoglobin, Result, Toxicity Grade
Item
Haemoglobin - Tox Grade
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Haematocrit
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C0518014 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Hematocrit level, Result
Item
Haematocrit - Result
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Hematocrit level, Result, Unit of Measure
Item
Haematocrit - Units
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Lower limit of reference range
Item
Haematocrit - Low
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Upper Limit of Normal
Item
Haematocrit - High
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Hematocrit level, Result, Toxicity Grade
Item
Haematocrit - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0518014 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Platelets
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C0005821 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Blood Platelets, Result
Item
Platelets - Result
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Blood Platelets, Result, Unit of Measure
Item
Platelets - Units
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Lower limit of reference range
Item
Platelets - Low
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Upper Limit of Normal
Item
Platelets - High
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Blood Platelets, Result, Toxicity Grade
Item
Platelets - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0005821 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
WBC
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, White Blood Cell Count procedure, Result
Item
WBC - Result
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, White Blood Cell Count procedure, Result, Unit of Measure
Item
WBC - Units
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Lower limit of reference range
Item
WBC - Low
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Upper Limit of Normal
Item
WBC - High
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, White Blood Cell Count procedure, Result, Toxicity Grade
Item
WBC - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0023508 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Differential Units
text
C0474523 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
CL Item
Precent (1)
CL Item
Absolute count (2)
Item
Basophils
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C0200641 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Blood basophil count (lab test), Result
Item
Basophils - Result
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Blood basophil count (lab test), Result, Unit of Measure
Item
Basophils - Units
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Lower limit of reference range
Item
Basophils - Low
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Upper Limit of Normal
Item
Basophils - High
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Blood basophil count (lab test), Result, Toxicity Grade
Item
Basophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0200641 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Eosinophils
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C0200638 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Eosinophil count procedure, Result
Item
Eosinophils - Result
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Eosinophil count procedure, Result, Unit of Measure
Item
Eosinophils - Units
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Lower limit of reference range
Item
Eosinophils - Low
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Upper Limit of Normal
Item
Eosinophils - High
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Eosinophil count procedure, Result, Toxicity Grade
Item
Eosinophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0200638 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Lymphocytes
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C0200635 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Lymphocyte Count measurement, Result
Item
Lymphocytes - Result
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Lymphocyte Count measurement, Result, Unit of Measure
Item
Lymphocytes - Units
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Lower limit of reference range
Item
Lymphocytes - Low
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Upper Limit of Normal
Item
Lymphocytes - High
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Lymphocyte Count measurement, Result, Toxicity Grade
Item
Lymphocytes - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0200635 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Monocytes
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C0750880 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Monocyte count result, Result
Item
Monocytes - Result
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Monocyte count result, Result, Unit of Measure
Item
Monocytes - Units
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Lower limit of reference range
Item
Monocytes - Low
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Upper Limit of Normal
Item
Monocytes - High
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Monocyte count result, Result, Toxicity Grade
Item
Monocytes - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0750880 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Item
Neutrophils
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C0948762 (UMLS CUI [1,2])
CL Item
No result (1)
CL Item
Results (2)
Hematology finding, Absolute neutrophil count, Result
Item
Neutrophils - Result
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Hematology finding, Absolute neutrophil count, Result, Unit of Measure
Item
Neutrophils - Units
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519795 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Lower limit of reference range
Item
Neutrophils - Low
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1272773 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Upper Limit of Normal
Item
Neutrophils - High
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Hematology finding, Absolute neutrophil count, Result, Toxicity Grade
Item
Neutrophils - Tox Grade
text
C0474523 (UMLS CUI [1,1])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
C0948762 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2826262 (UMLS CUI [1,4])
Laboratory Procedures, Hematology finding, Laboratory, Other
Item
Was any test on this page performed at a different lab than specified on this page?
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0474523 (UMLS CUI [1,2])
C0022877 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Clinical Trial Subject Unique Identifier
Item
Subject number
integer
C2348585 (UMLS CUI [1])
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