Item
Initial Report
integer
C0684224 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
Item
Follow-Up Report
integer
C1704685 (UMLS CUI [1])
Code List
Follow-Up Report
SAE Sequence number
Item
SAE Sequence number
text
C1519255 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Serious Adverse event
Item
Serious Adverse event
text
C1519255 (UMLS CUI [1])
Serious Adverse event, Modified term
Item
Modified term
text
C1519255 (UMLS CUI [1,1])
C2826798 (UMLS CUI [1,2])
SAE MedDRA synonym
Item
MedDRA synonym
text
C1519255 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
SAE MedDRA lower level term code
Item
MedDRA lower level term code
text
C1519255 (UMLS CUI [1,1])
C3898442 (UMLS CUI [1,2])
Failed coding
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
SAE Start Date and Time
Item
Serious Adverse Event Start Date and Time
partialDatetime
C1519255 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C1301880 (UMLS CUI [2,2])
Item
Serious Adverse Event Outcome
integer
C1705586 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
Code List
Serious Adverse Event Outcome
CL Item
Recovered/Resolved, provide End Date and Time (1)
CL Item
Recovering/Resolving (2)
CL Item
Not recovered/not resolved (3)
CL Item
Recovered/Resolved with sequelae, provide End Date and Time (4)
CL Item
Fatal, record Date and Time of Death (5)
SAE End Date and Time if Recovered/Resolved
Item
If recovered/Resolved, provide End Date and Time
partialDatetime
C1519255 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
C1709863 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C1522314 (UMLS CUI [2,2])
C1709863 (UMLS CUI [2,3])
SAE End Date and Time if Recovered/Resolved with sequelae
Item
If recovered/Resolved with sequelae, provide End Date and Time
partialDatetime
C1519255 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
C1709863 (UMLS CUI [1,3])
C0243088 (UMLS CUI [1,4])
C1519255 (UMLS CUI [2,1])
C1522314 (UMLS CUI [2,2])
C1709863 (UMLS CUI [2,3])
C0243088 (UMLS CUI [2,4])
SAE Date and Time of Death
Item
If Fatal, record Date and Time of Death
partialDatetime
C1519255 (UMLS CUI [1,1])
C3899439 (UMLS CUI [1,2])
Item
Maximum Intensity
text
C1519255 (UMLS CUI [1,1])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
Code List
Maximum Intensity
CL Item
Not applicable (X)
Item
Intensity at onset of event
text
C1519255 (UMLS CUI [1,1])
C0518690 (UMLS CUI [1,2])
C0332162 (UMLS CUI [1,3])
Code List
Intensity at onset of event
CL Item
Not applicable (X)
Item
Maximum Grade of Serious Adverse Event
integer
C1519255 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
Code List
Maximum Grade of Serious Adverse Event
Item
Grade at onset of event
integer
C1519255 (UMLS CUI [1,1])
C0806909 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C0332162 (UMLS CUI [1,4])
Code List
Grade at onset of event
Item
Maximum Grade or Intensity of Serious Adverse Event
text
C1519255 (UMLS CUI [1,1])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0441800 (UMLS CUI [2,2])
C0806909 (UMLS CUI [2,3])
Code List
Maximum Grade or Intensity of Serious Adverse Event
CL Item
Mild or Grade 1 (1)
CL Item
Moderate or Grade 2 (2)
CL Item
Severe or Grade 3 (3)
CL Item
Not applicable (X)
Item
Grade or Intensity at onset of event
text
C0518690 (UMLS CUI [1,1])
C0332162 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C0441800 (UMLS CUI [2,1])
C0332162 (UMLS CUI [2,2])
C1519255 (UMLS CUI [2,3])
Code List
Grade or Intensity at onset of event
CL Item
Mild or Grade 1 (1)
CL Item
Moderate or Grade 2 (2)
CL Item
Severe or Grade 3 (3)
CL Item
Not applicable (X)
Item
Action taken with Investigational Product(s) as a result of AE?
text
C1519255 (UMLS CUI [1,1])
C2826626 (UMLS CUI [1,2])
Code List
Action taken with Investigational Product(s) as a result of AE?
CL Item
Investigational product(s) withdrawn (1)
CL Item
Dose increased (3)
CL Item
Dose not changed (4)
CL Item
Dose interrupted (5)
CL Item
Not applicable (X)
Item
Did the subject withdraw from the study as a result of AE?
text
C0422727 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
Code List
Did the subject withdraw from the study as a result of AE?
Item
Is there a reasonable possibility that the AE may have been caused by the investigational product?
text
C1519255 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
Code List
Is there a reasonable possibility that the AE may have been caused by the investigational product?
Duration of SAE if < 24 hours
Item
Duration of AE if < 24 hours
text
C1519255 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
SAE Time to Onset since last Dose
Item
Time to Onset since last Dose
time
C1519255 (UMLS CUI [1,1])
C0449244 (UMLS CUI [1,2])
C0946444 (UMLS CUI [1,3])
Item
Was the SAE caused by activities related to study participation other than investigational product (e.g., procedures, blood draws, washout, etc)?
text
C1519255 (UMLS CUI [1,1])
C0085978 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0085978 (UMLS CUI [2,2])
C2700391 (UMLS CUI [2,3])
C1519255 (UMLS CUI [3,1])
C0085978 (UMLS CUI [3,2])
C0005834 (UMLS CUI [3,3])
C1519255 (UMLS CUI [4,1])
C0085978 (UMLS CUI [4,2])
C1710661 (UMLS CUI [4,3])
C0332197 (UMLS CUI [5,1])
C0304229 (UMLS CUI [5,2])
Code List
Was the SAE caused by activities related to study participation other than investigational product (e.g., procedures, blood draws, washout, etc)?
Item
Was the event serious?
text
C1710056 (UMLS CUI [1])
Code List
Was the event serious?
SAE Related Investigational Product
Item
Related Investigational Product
text
C1519255 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
Serious Adverse Event
Item
Serious Adverse Event
text
C1519255 (UMLS CUI [1])
Start Date and Time of SAE segment
Item
Start Date and Time of event segment
partialDatetime
C1519255 (UMLS CUI [1,1])
C0449719 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0449719 (UMLS CUI [2,2])
C1301880 (UMLS CUI [2,3])
Item
Intensity of event segment
integer
C1519255 (UMLS CUI [1,1])
C0449719 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
Code List
Intensity of event segment
Item
Grade of event segment
integer
C1519255 (UMLS CUI [1,1])
C2985911 (UMLS CUI [1,2])
C0449719 (UMLS CUI [1,3])
Code List
Grade of event segment
Item
Grade or Intensity of event segment
integer
C1519255 (UMLS CUI [1,1])
C0518690 (UMLS CUI [1,2])
C0449719 (UMLS CUI [1,3])
C2985911 (UMLS CUI [2])
Code List
Grade or Intensity of event segment
CL Item
Mild or Grade l (1)
CL Item
Moderate or Grade 2 (2)
CL Item
Severe or Grade 3 (3)
SAE seriousness: Results in death
Item
Seriousness? [A] Results in death
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1705232 (UMLS CUI [2,1])
C1519255 (UMLS CUI [2,2])
SAE seriousness: Is life-threatening
Item
Seriousness? [B] Is life-threatening
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1517874 (UMLS CUI [2,1])
C1519255 (UMLS CUI [2,2])
SAE seriousness: Requires hospitalisation or prolongation of existing hospitalisation
Item
Seriousness? [C] Requires hospitalisation or prolongation of existing hospitalisation
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C0019993 (UMLS CUI [2,2])
C1519255 (UMLS CUI [3,1])
C0745041 (UMLS CUI [3,2])
SAE seriousness: Results in disability/incapacity
Item
Seriousness? [D] Results in disability/incapacity
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C0231170 (UMLS CUI [2,2])
C1519255 (UMLS CUI [3,1])
C3176592 (UMLS CUI [3,2])
SAE seriousness: Congenital anomaly
Item
Seriousness? [E] Congenital anomaly/birth defect
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C0000768 (UMLS CUI [2,1])
C1519255 (UMLS CUI [2,2])
SAE seriousness: Other, specify
Item
Seriousness? [F] Other, specify within general narrative comment
boolean
C0205394 (UMLS CUI [1,1])
C1710056 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
SAE seriousness: Cardiovascular or hepatobiliary events
Item
Seriousness? [G] Cardiovascular or hepatobiliary events (Refer to Section 12.2.1 of the Protocol.)
boolean
C1710056 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1320716 (UMLS CUI [2,1])
C1519255 (UMLS CUI [2,2])
C0267792 (UMLS CUI [3,1])
C1519255 (UMLS CUI [3,2])
SAE relevant Medication Sequence number
Item
CM Sequence number
integer
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,4])
SAE relevant Drug name
Item
Drug name
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
SAE relevant Modified reported term
Item
Modified reported term
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826302 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
SAE relevant Drug Dose
Item
Drug Dose
integer
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0869039 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
Item
Dose unit
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0869039 (UMLS CUI [1,3])
CL Item
Cubic centimeter (CC)
CL Item
International units (025)
CL Item
International units per kilogram (028)
CL Item
International units per millilitre (IUML)
CL Item
Litre per minute (LM)
CL Item
Megaunits (million units) (MEGU)
CL Item
Microgram (UG) (004)
CL Item
Microgram (UG) (004)
CL Item
Microgram/kilogram (008)
CL Item
Microgram/kilogram per minute (MCG/KG/MIN)
CL Item
Micrograms per minute (MCG/MIN)
CL Item
Milliequivalent (029)
CL Item
Milliequivalent per 24 hours (MEQ24)
CL Item
Milligrams percent (MGPER)
CL Item
Milligram per hour (MGH)
CL Item
Milligram/kilogram (007)
CL Item
Milligram/kilogram per hour (MGKH)
CL Item
Milligram/kilogram per minute (MGKM)
CL Item
Milligram/metre squared (009)
CL Item
Milligram/millilitre (MGML)
CL Item
Millilitre per hour (MLH)
CL Item
Millilitre per minute (MLM)
CL Item
Million International units (027)
CL Item
Minimum alveolar concentration (MAC)
CL Item
Suppository (SUP)
Item
Frequency
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C3476109 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
CL Item
2 times per week (2W)
CL Item
3 times per week (3W)
CL Item
4 times per week (4W)
CL Item
5 times per day (5D)
CL Item
5 times per week (5W)
CL Item
Continuous infusion (CO)
CL Item
Every 2 weeks (FO)
CL Item
Every 3 weeks (Q3WK)
CL Item
Every 3 months (Q3M)
CL Item
Every other day (AD)
CL Item
Once a month (MO)
Item
Route
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
CL Item
Gastrostomy tube (GT)
CL Item
Intra-arterial (013)
CL Item
Intra-bursa (IBU)
CL Item
Intralesional (026)
CL Item
Intramuscular (030)
CL Item
Intraocular (031)
CL Item
lntraosteal (IOS)
CL Item
Intraperitoneal (033)
CL Item
Intrathecal (037)
CL Item
Intrauterine (015)
CL Item
Intravenous (042)
CL Item
Subcutaneous (058)
CL Item
Transdermal (062)
SAE relevant medication Start Date
Item
Date started
date
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
Item
Ongoing?
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
CL Item
No, specify End Date (N)
SAE relevant Medication End Date
Item
If not ongoing, specify End Date
partialDate
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,4])
Primary indication of SAE relevant medication
Item
Primary indication
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
SAE relevant Modified reported term
Item
Modified reported term
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826923 (UMLS CUI [1,3])
Item
Drug type
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0457591 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
SAE relevant MHx Sequence Number
Item
MHx Sequence Number
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C0262926 (UMLS CUI [1,4])
SAE relevant Specific Condition Name
Item
Specific Condition Name
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
SAE relevant Modified reported term
Item
Modified reported term
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826923 (UMLS CUI [1,3])
Date of onset of risk factors or disease relevant to SAE
Item
Date of onset
partialDate
C0574845 (UMLS CUI [1,1])
C0035648 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,4])
C0574845 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C2347946 (UMLS CUI [2,3])
C1519255 (UMLS CUI [2,4])
Item
Is medical condition continuing?
integer
C0012634 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,4])
Code List
Is medical condition continuing?
CL Item
No, specify date of last occurrence (2)
Date of last occurence of disease relevant to SAE
Item
If NO, specify date of last occurrence
partialDate
C0011008 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,4])
C2347946 (UMLS CUI [1,5])
C1519255 (UMLS CUI [1,6])
Other SAE Relevant Medical History / Risk Factors
Item
Relevant Medical History / Risk Factors not noted above
text
C0205394 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,4])
C0205394 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C0035648 (UMLS CUI [2,3])
C1519255 (UMLS CUI [2,4])
SAE relevant Lab Sequence Number
Item
Lab Sequence Number
integer
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0022885 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,4])
Item
Test Name
integer
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0022885 (UMLS CUI [1,3])
CL Item
Activated partial thromboplastin time (1)
CL Item
Alkaline phosphatase (3)
CL Item
Bilirubin direct (8)
CL Item
Blllrubln total (9)
CL Item
Blood myoglobin (10)
CL Item
Blood pressure (12)
CL Item
Blood urea nitrogen (13)
CL Item
Body temperature (14)
CL Item
CD4 lymphocytes (16)
CL Item
CD8 lymphocytes (17)
CL Item
Cholesterol total (19)
CL Item
C-reactive protein (20)
CL Item
Creatine phosphokinase (22)
CL Item
Creatine phosphokinase MB (23)
CL Item
Creatinine clearance (25)
CL Item
Diastolic blood pressure (26)
CL Item
Erythrocyte sedimentation rate (28)
CL Item
Fasting blood glucose (29)
CL Item
Gamma-glutamyltransferase (31)
CL Item
Glutamic-oxaloacetic transferase (32)
CL Item
Glutamic-pyruvate transaminase (33)
CL Item
HBV-DNA decreased (35)
CL Item
HBV-DNA Increased (36)
CL Item
High density lipoprotein (40)
CL Item
HIV viral load (41)
CL Item
lactic dehydrogenase (43)
CL Item
Low density lipoprotein (45)
CL Item
Mean cell hemoglobin concentration (48)
CL Item
Mean corpuscular hemoglobin (49)
CL Item
Mean corpuscular volume (50)
CL Item
Oxygen saturation (53)
CL Item
Platelet count (57)
CL Item
Protein total (60)
CL Item
Prothrombin time (61)
CL Item
Red blood cell count (62)
CL Item
Respiratory rate (63)
CL Item
Reticulocyte count (64)
CL Item
Serum glucose (65)
CL Item
Serum uric acid (66)
CL Item
Systolic blood pressure (68)
CL Item
Thrombin time (69)
CL Item
Total lung capacity (70)
CL Item
Triglycerides (71)
CL Item
Urine myoglobin (75)
CL Item
Vital capacity (77)
CL Item
White blood cell count (78)
SAE relevant Laboratory Test Date
Item
Test Date
partialDate
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826641 (UMLS CUI [1,3])
SAE relevant Laboratory Test Result
Item
Test Result
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,3])
SAE relevant Laboratory Test Units
Item
Test Units
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C0587081 (UMLS CUI [1,4])
SAE relevant Laboratory Test Normal Low Range
Item
Normal Low Range
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826705 (UMLS CUI [1,3])
C1518030 (UMLS CUI [1,4])
SAE relevant Laboratory Test Normal High Range
Item
Normal High Range
text
C1519255 (UMLS CUI [1,1])
C2347946 (UMLS CUI [1,2])
C2826705 (UMLS CUI [1,3])
C1519815 (UMLS CUI [1,4])
Other diagnostic test results relevant to SAE
Item
Relevant diagnostic results not noted above
text
C0430022 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,4])
C0205394 (UMLS CUI [1,5])
Item
If the investigational product(s) were stopped temporarily, did the reported event(s) recur after investigational products were restarted?
text
C0034897 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C2347900 (UMLS CUI [1,4])
C0687676 (UMLS CUI [1,5])
C0457454 (UMLS CUI [1,6])
Code List
If the investigational product(s) were stopped temporarily, did the reported event(s) recur after investigational products were restarted?
CL Item
Unknown at this time (U)
CL Item
Not applicable (X)
Item
Study Drug
text
C0304229 (UMLS CUI [1])
Start Date
Item
Study Drug Start Date
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Stop Date
Item
Study Drug Stop Date
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Therapeutic regimen of experimental drug
Item
Regimen
text
C1276413 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
General narrative comments
Item
General narrative comments
text
C0947611 (UMLS CUI [1])
Item
Send incomplete SAE data to GSK Safety
integer
C1519255 (UMLS CUI [1,1])
C1511726 (UMLS CUI [1,2])
C0205257 (UMLS CUI [1,3])
Code List
Send incomplete SAE data to GSK Safety
CL Item
Incomplete SAE (3)
SAE data: Receipt by GSK date
Item
Receipt by GSK date
partialDatetime
C2985846 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1511726 (UMLS CUI [1,3])
Item
Was the event serious?
text
C1710056 (UMLS CUI [1])
Code List
Was the event serious?
SAE Sequence number
Item
SAE Sequence number
text
C1519255 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Version Number of SAE Data
Item
Version Number
text
C0333052 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C1511726 (UMLS CUI [1,4])
Case ID
Item
Case ID
text
C1698493 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Randomisation Number
Item
Randomisation Number
text
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
OCEANS Code
Item
OCEANS Code
text
C0805701 (UMLS CUI [1,1])
C3887242 (UMLS CUI [1,2])
SAE Data Email Flag
Item
Email Flag
text
C1519255 (UMLS CUI [1,1])
C1511726 (UMLS CUI [1,2])
C0013849 (UMLS CUI [1,3])