ID
36722
Beschrijving
ICHOM Hypertension in low- and middle-income countries data collection Version 1.0.0 Revised: November 3rd, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ The following condition and treatment approaches (or interventions) are covered by our Standard Set. Condition: Hypertension (ICD-10: I10) Treatment Approaches: Pharmacological and Non-Pharmacological Collecting Patient-Reported Outcome Measures: Survey Used: EuroQol-5D-3L (EQ-5D-3L). As a licence is needed for use of EQ-5D-3L questionnaires, the actual questions are not part of this version of the standard set. For licensing information see: https://euroqol.org/support/how-to-obtain-eq-5d/ This document contains the Annually - Clinical Form. It has to be filled in one year after patient's entry into set and annually for life. PROMIS Single Question on erectile Dysfunction. Free for use in clinical practice. As http://www.nihpromis.org/ is the official distribution site for PROMIS questionnaires and translations, only the total score will be included in this version of the standard set. Beliefs about Medication Questionnaire (BMQ)-Specific: Copyrighted, permission to use the scale can be obtained from Professor Rob Horne’s research team. The scoring guide can be found in the original validation article: Horne et al. (1999) The beliefs about medicines questionnaire: The development and evaluation of a new method for assessing the cognitive representation of medication. Psychology & Health, 14:1. Hill-Bone Compliance to High Blood Pressure Therapy Scale - South Africa Version: Permission to use the scale can be obtained from Estelle V. Lambert’s research team, The scoring guide can be found in the original validation article: Lambert, E.V. et al. (2006) Cross-Cultural Validation of the Hill-Bone Compliance To High Blood Pressure Therapy Scale in a South African, Primary Healthcare Setting. Ethnicity and Disease, 16. WHO STEPS Instrument. Free for use in clinical practice and a license is not required. http://www.who.int/chp/steps/instrument/en/ International Physical Activity Questionnaire(IPAQ)-Short Form: Publically available, open access, and no permissions are required to use it. https://sites.google.com/site/theipaq/ Alternative Quality of Life Surveys: PROMIS Global-10 Free for use in clinical practice. As http://www.nihpromis.org/ is the official distribution site for PROMIS questionnaires and translations, only the total score will be included in this version of the standard set. Veteran’s Rand 12-Item Health Survey (VR-12). Free for all health care organizations, license required and can be requested at: http://bit.ly/2ir84sG. As a license is needed, the actual questions are not part of this version of the standard set. 12-Item Short Form Survey (SF-12). As a license is needed for use of SF-12 questionaires, the actual questions are not part of this version of the standard set. For more information see: http://bit.ly/2AcNLrme This Standard set was supported by the Novartis Foundation.
Link
Trefwoorden
Versies (3)
- 04-06-19 04-06-19 -
- 04-06-19 04-06-19 - Sarah Riepenhausen
- 30-04-20 30-04-20 - Sarah Riepenhausen
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ICHOM
Geüploaded op
4 juni 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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ICHOM Hypertension in low- and middle-income countries
Annually - Clinical Form
- StudyEvent: ODM
Beschrijving
Clinical Factors
Alias
- UMLS CUI-1
- C0449440
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and annually until positive diagnosis of diabetes Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0011849
- UMLS CUI [2,1]
- C0011849
- UMLS CUI [2,2]
- C1518321
Beschrijving
Supporting Definition: Fasting plasma glucose value in mg/dL or mmol/L Inclusion Criteria: Optional Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Numerical Response Options: N/A
Datatype
float
Alias
- UMLS CUI [1]
- C0583513
Beschrijving
Inclusion Criteria: If fasting plasma glucose value is provided Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0583513
- UMLS CUI [1,2]
- C1519795
Beschrijving
Supporting Definition: Height and weight are used to calculate BMI Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-reported Type: Numerical Response Options: Numerical value
Datatype
float
Alias
- UMLS CUI [1]
- C0005910
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Beschrijving
Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0585943
Beschrijving
Inclusion Criteria: If answered 1 to LIPIDLOW Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0585943
- UMLS CUI [1,2]
- C2348235
Beschrijving
Inclusion Criteria: Optional Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0201976
Beschrijving
Supporting Definition: Please provide the most recent value Inclusion Criteria: If responded "yes" to CREADONE Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Numerical, enter "000" if unknown Response Options: Numerical value
Datatype
float
Alias
- UMLS CUI [1,1]
- C0201976
- UMLS CUI [1,2]
- C1274040
Beschrijving
Inclusion Criteria: If value for creatinine is provided Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0201976
- UMLS CUI [1,2]
- C1519795
Beschrijving
Inclusion Criteria: If value for creatinine is provided Timing: Baseline and annually Reporting Source: Clinician-reported/administratively‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0201976
- UMLS CUI [1,2]
- C0006751
- UMLS CUI [1,3]
- C3274766
Beschrijving
Treatment variables
Alias
- UMLS CUI-1
- C0087111
Beschrijving
Supporting Definition: Non‐pharmacological management includes lifestyle interventions, exercise, diet and other non-pharmacological approaches. Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0449445
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0003015
- UMLS CUI [3]
- C0521942
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0001641
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0001645
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0354100
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0012802
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0006684
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0205394
Beschrijving
Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0003364
- UMLS CUI [1,2]
- C0596463
- UMLS CUI [2]
- C0439673
Beschrijving
Survival, disease control and cardiovascular complications
Alias
- UMLS CUI-1
- C1148433
- UMLS CUI-2
- C0012634
- UMLS CUI-3
- C0243148
- UMLS CUI-4
- C0007226
- UMLS CUI-5
- C0009566
Beschrijving
Inclusion Criteria: All patients Timing: Minimum annually Reporting Source: Clinician‐reported Type: Numerical Response Options: Numerical value
Datatype
integer
Maateenheden
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschrijving
Inclusion Criteria: All patients Timing: Minimum annually Reporting Source: Clinician‐reported Type: Numerical Response Options: Numerical value
Datatype
integer
Maateenheden
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschrijving
Inclusion Criteria: All patients Timing: At time of death Reporting Source: Clinician-reported/administratively‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0011065
Beschrijving
Inclusion Criteria: If answered 'yes' to overall survival (OVERALLSURV) Timing: At time of death Reporting Source: Clinician-reported/administratively‐reported Type: Date by DD/MM/YYYY or by MM/YYYY (in case exact day is unknown) Response Options: DD/MM/YYYY or MM/YYYY
Datatype
date
Alias
- UMLS CUI [1]
- C1148348
Beschrijving
Inclusion Criteria: If answered 'yes' to overall survival (OVERALLSURV) Timing: At time of death Reporting Source: Clinician-reported/administratively‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0007465
Beschrijving
Inclusion Criteria: All patients Timing: Annually and 4-‐6 weeks after initiation or change of treatment Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0392325
- UMLS CUI [2]
- C0877248
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0085639
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C2609414
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0085649
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0015672
- UMLS CUI [3,1]
- C2700116
- UMLS CUI [3,2]
- C0848717
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0151613
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0020621
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0010200
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0242350
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0042023
Beschrijving
Supporting Definition: Hypotension and clinical manifestations of hypotension Inclusion Criteria: If answered 'yes' to medication side effects ('MEDEFFECTS') Timing: Annually and 4-6 weeks after initiation or change of treatment Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0205394
Beschrijving
Supporting Definition: Myocardial infarction (ICD10: I21) or angina (ICD10: I20) diagnosed by a clinician Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1869045
Beschrijving
Supporting Definition: Cerebrovascular accident (ICD10: I60 ‐ Subarachnoid haemorrhage, I61 – Intracerebral haemorrhage, I62 – other non-‐traumatic intracranial haemorrhage, I63 – cerebral infarction, I64 -‐ Stroke, not specified as haemorrhage or infarction) or transient ischaemic attack (ICD10: G45 ‐ Transient cerebral ischaemic attacks and related syndromes) diagnosed by a clinician Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0007820
Beschrijving
Supporting Definition: Atrial fibrillation (ICD10: I48.0 paroxysmal atrial fibrillation, I48.1 – persistent atrial fibrillation, I48.2 Chronic atrial fibrillation) diagnosed by a clinician Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0004238
Beschrijving
Supporting Definition: Heart failure (ICD10: I50 ‐ Heart failure, ICD:10 I11.0 – hypertensive heart disease with (congestive) heart failure) diagnosed by a clinician Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0018801
Beschrijving
Inclusion Criteria: If answered 'yes' to heart failure ('HF') Timing: Annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0085978
- UMLS CUI [1,2]
- C0018801
Beschrijving
Supporting Definition: Peripheral artery disease (ICD:10 I70.2 -‐ Atherosclerosis of arteries of extremities) diagnosed by clinician Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1704436
Beschrijving
Supporting Definition: Renal disease (ICD10: I12 Hypertensive renal disease incl. any condition in N00-‐ N07, N18.-‐, N19 or N26 due to hypertension) (Please ensure that other causes of proteinuria, such as urinary tract infection, have been ruled out) Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1561643
- UMLS CUI [2]
- C0033687
Beschrijving
Inclusion Criteria: If "yes" to CKD Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0033687
- UMLS CUI [1,2]
- C3887511
Beschrijving
Inclusion Criteria: If responded "1" or "2" to PROTEINEVID Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single response
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C1160927
Beschrijving
Inclusion Criteria: If responded "3" to PROTEINEVID Timing: Baseline and annually Reporting Source: Clinician-reported Type: Numerical Response Options: Numerical value
Datatype
float
Alias
- UMLS CUI [1,1]
- C0455271
- UMLS CUI [1,2]
- C2826772
Beschrijving
Inclusion Criteria: If ACR value provided Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0455271
- UMLS CUI [1,2]
- C1519795
Beschrijving
Supporting Definition: Hypertensive urgency is an acute rise in BP >180/120 mmHg with no evidence of acute end-organ damage. Hypertensive emergency is an acute rise in BP > 180/120 with evidence of acute end organ damage. Inclusion Criteria: All patients Timing: Annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0745138
- UMLS CUI [2]
- C0745136
Beschrijving
Inclusion Criteria: If answered 'yes' to hypertensive urgency/ hypertensive emergency ('HYPTENEMERG') Timing: Annually Reporting Source: Clinician‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0205178
- UMLS CUI [1,2]
- C0743496
Beschrijving
Inclusion Criteria: If answered 'yes' to acute end-‐organ damage ('HYPTENENDORG') Timing: Annually Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0205178
- UMLS CUI [1,3]
- C0743496
- UMLS CUI [2]
- C0015397
Beschrijving
Inclusion Criteria: If answered 'yes' to acute end-‐organ damage ('HYPTENENDORG') Timing: Annually Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0205178
- UMLS CUI [1,3]
- C0743496
- UMLS CUI [2]
- C0022646
Beschrijving
Inclusion Criteria: If answered 'yes' to acute end-‐organ damage ('HYPTENENDORG') Timing: Annually Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0205178
- UMLS CUI [1,3]
- C0743496
- UMLS CUI [2]
- C1522601
Beschrijving
Inclusion Criteria: If answered 'yes' to acute end-‐organ damage ('HYPTENENDORG') Timing: Annually Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0205178
- UMLS CUI [1,3]
- C0743496
- UMLS CUI [2]
- C1880018
Beschrijving
Inclusion Criteria: If answered 'yes' to acute end-‐organ damage ('HYPTENENDORG') Timing: Annually Reporting Source: Clinician-reported Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0205178
- UMLS CUI [1,3]
- C0743496
- UMLS CUI [2]
- C0439673
Beschrijving
Health status
Alias
- UMLS CUI-1
- C0018759
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Annually - Clinical Form
- StudyEvent: ODM
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C0596463 (UMLS CUI [1,2])
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C0430022 (UMLS CUI-2)
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C0392325 (UMLS CUI [1,2])
C0085639 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C2609414 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0085649 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0015672 (UMLS CUI [2])
C2700116 (UMLS CUI [3,1])
C0848717 (UMLS CUI [3,2])
C0392325 (UMLS CUI [1,2])
C0151613 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0020621 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0010200 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0242350 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0042023 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2])
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C0018801 (UMLS CUI [1,2])
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C0033687 (UMLS CUI [2])
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C3887511 (UMLS CUI [1,2])
C2911685 (UMLS CUI-2)
C0175674 (UMLS CUI-3)
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C2911685 (UMLS CUI-2)
C0022885 (UMLS CUI-3)
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C1160927 (UMLS CUI [1,2])
C1254595 (UMLS CUI-2)
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C2826772 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
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C0745136 (UMLS CUI [2])
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C0743496 (UMLS CUI [1,2])
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C0205178 (UMLS CUI [1,2])
C0743496 (UMLS CUI [1,3])
C0015397 (UMLS CUI [2])
C0205178 (UMLS CUI [1,2])
C0743496 (UMLS CUI [1,3])
C0022646 (UMLS CUI [2])
C0205178 (UMLS CUI [1,2])
C0743496 (UMLS CUI [1,3])
C1522601 (UMLS CUI [2])
C0205178 (UMLS CUI [1,2])
C0743496 (UMLS CUI [1,3])
C1880018 (UMLS CUI [2])
C0205178 (UMLS CUI [1,2])
C0743496 (UMLS CUI [1,3])
C0439673 (UMLS CUI [2])
C0449820 (UMLS CUI [1,2])
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