English

Observation Class: Relationships - Domain: Related Records

59 forms  
  1. StudyEvent: ODM
    1. Observation Class: Special Purpose - Domain: Comments
    2. Observation Class: Special Purpose - Domain: Demographics
    3. Observation Class: Special Purpose - Domain: Subject Elements
    4. Observation Class: Special Purpose - Domain: Subject Disease Milestones
    5. Observation Class: Special Purpose - Domain: Subject Visits
    6. Observation Class: Interventions - Domain: Procedure Agents
    7. Observation Class: Interventions - Domain: Concomitant/Prior Medications
    8. Observation Class: Interventions - Domain: Exposure
    9. Observation Class: Interventions - Domain: Exposure as Collected
    10. Observation Class: Interventions - Domain: Meal Data
    11. Observation Class: Interventions - Domain: Procedures
    12. Observation Class: Interventions - Domain: Substance Use
    13. Observation Class: Events - Domain: Adverse Events
    14. Observation Class: Events - Domain: Clinical Events
    15. Observation Class: Events - Domain: Disposition
    16. Observation Class: Events - Domain: Protocol Deviations
    17. Observation Class: Events - Domain: Healthcare Encounters
    18. Observation Class: Events - Domain: Medical History
    19. Observation Class: Findings - Domain: Drug Accountability
    20. Observation Class: Findings - Domain: Death Details
    21. Observation Class: Findings - Domain: ECG Test Results
    22. Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met
    23. Observation Class: Findings - Domain: Immunogenicity Specimen Assessments
    24. Observation Class: Findings - Domain: Laboratory Test Results
    25. Observation Class: Findings - Domain: Microbiology Specimen
    26. Observation Class: Findings - Domain: Microbiology Susceptibility
    27. Observation Class: Findings - Domain: Microscopic Findings
    28. Observation Class: Findings - Domain: Morphology
    29. Observation Class: Findings - Domain: Cardiovascular System Findings
    30. Observation Class: Findings - Domain: Musculoskeletal System Findings
    31. Observation Class: Findings - Domain: Nervous System Findings
    32. Observation Class: Findings - Domain: Ophthalmic Examinations
    33. Observation Class: Findings - Domain: Reproductive System Findings
    34. Observation Class: Findings - Domain: Respiratory System Findings
    35. Observation Class: Findings - Domain: Urinary System Findings
    36. Observation Class: Findings - Domain: Pharmacokinetics Concentrations
    37. Observation Class: Findings - Domain: Pharmacokinetics Parameters
    38. Observation Class: Findings - Domain: Physical Examination
    39. Observation Class: Findings - Domain: Functional Tests
    40. Observation Class: Findings - Domain: Questionnaires
    41. Observation Class: Findings - Domain: Disease Response and Clin Classification
    42. Observation Class: Findings - Domain: Subject Characteristics
    43. Observation Class: Findings - Domain: Subject Status
    44. Observation Class: Findings - Domain: Tumor/Lesion Identification
    45. Observation Class: Findings - Domain: Tumor/Lesion Results
    46. Observation Class: Findings - Domain: Vital Signs
    47. Observation Class: Findings - Domain: Findings About Events or Interventions
    48. Observation Class: Findings - Domain: Skin Response
    49. Observation Class: Trial Design - Domain: Trial Arms
    50. Observation Class: Trial Design - Domain: Trial Elements
    51. Observation Class: Trial Design - Domain: Trial Visits
    52. Observation Class: Trial Design - Domain: Trial Disease Assessments
    53. Observation Class: Trial Design - Domain: Trial Disease Milestones
    54. Observation Class: Trial Design - Domain: Trial Inclusion/Exclusion Criteria
    55. Observation Class: Trial Design - Domain: Trial Summary Information
    56. Observation Class: Relationships - Domain: Related Records
    57. Observation Class: Relationships - Domain: Supplemental Qualifiers for [domain name]
    58. Observation Class: Relationships - Domain: Related Subjects
    59. Observation Class: Study Reference - Domain: Non-host Organism Identifiers
Related Records
Description

Related Records

Alias
SDTMIG v3.3
RELREC
NCIt V19.10d:
C147182
UMLS CUI-1
C4687766
Study Identifier
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Unique identifier for a study. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1]
C2826693
SDTMIG 3.3
STUDYID
NCIt V19.10d
C83082
Related Domain Abbreviation
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Abbreviation for the domain of the parent record(s). Controlled Terms or Format (if applicable): (DOMAIN), extensible

Data type

text

Alias
UMLS CUI [1,1]
C0439849
UMLS CUI [1,2]
C1883204
UMLS CUI [1,3]
C0000723
SDTMIG 3.3
RDOMAIN
NCIt V19.10d
C2826980
Unique Subject Identifier
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Identifier used to uniquely identify a subject across all studies for all applications or submissions involving the product. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C1710548
UMLS CUI [1,2]
C2826693
SDTMIG 3.3
USUBJID
NCIt V19.10d
C70731
Identifying Variable
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Name of the identifying variable in the general-observation-class dataset that identifies the related record(s). Examples include --SEQ and --GRPID. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0439828
SDTMIG 3.3
IDVAR
NCIt V19.10d
C83293
Identifying Variable Value
Description

Role: Identifier CDISC Notes (for domains) Description (for General Classes): Value of identifying variable described in IDVAR. If --SEQ is the variable being used to describe this record, then the value of --SEQ would be entered here. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0439828
SDTMIG 3.3
IDVARVAL
NCIt V19.10d
C83294
Relationship Type
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): Identifies the hierarchical level of the records in the relationship. Values should be either ONE or MANY. Used only when identifying a relationship between datasets (as described in Section 8.3, Relating Datasets). Controlled Terms or Format (if applicable): (RELTYPE), not extensible

Data type

text

Alias
UMLS CUI [1,1]
C0439849
UMLS CUI [1,2]
C0332307
SDTMIG 3.3
RELTYPE
NCIt V19.10d
C83393
Relationship Identifier
Description

Role: Record Qualifier CDISC Notes (for domains) Description (for General Classes): Unique value within USUBJID that identifies the relationship. All records for the same USUBJID that have the same RELID are considered "related/associated." RELID can be any value the sponsor chooses, and is only meaningful within the RELREC dataset to identify the related/associated Domain records. Controlled Terms or Format (if applicable): NA

Data type

text

Alias
UMLS CUI [1,1]
C0439849
UMLS CUI [1,2]
C0600091
SDTMIG 3.3
RELID
NCIt V19.10d
C83392
Back to the top of the page

Similar models

Observation Class: Relationships - Domain: Related Records

59 forms
  1. StudyEvent: ODM
    1. Observation Class: Special Purpose - Domain: Comments
    2. Observation Class: Special Purpose - Domain: Demographics
    3. Observation Class: Special Purpose - Domain: Subject Elements
    4. Observation Class: Special Purpose - Domain: Subject Disease Milestones
    5. Observation Class: Special Purpose - Domain: Subject Visits
    6. Observation Class: Interventions - Domain: Procedure Agents
    7. Observation Class: Interventions - Domain: Concomitant/Prior Medications
    8. Observation Class: Interventions - Domain: Exposure
    9. Observation Class: Interventions - Domain: Exposure as Collected
    10. Observation Class: Interventions - Domain: Meal Data
    11. Observation Class: Interventions - Domain: Procedures
    12. Observation Class: Interventions - Domain: Substance Use
    13. Observation Class: Events - Domain: Adverse Events
    14. Observation Class: Events - Domain: Clinical Events
    15. Observation Class: Events - Domain: Disposition
    16. Observation Class: Events - Domain: Protocol Deviations
    17. Observation Class: Events - Domain: Healthcare Encounters
    18. Observation Class: Events - Domain: Medical History
    19. Observation Class: Findings - Domain: Drug Accountability
    20. Observation Class: Findings - Domain: Death Details
    21. Observation Class: Findings - Domain: ECG Test Results
    22. Observation Class: Findings - Domain: Inclusion/Exclusion Criteria Not Met
    23. Observation Class: Findings - Domain: Immunogenicity Specimen Assessments
    24. Observation Class: Findings - Domain: Laboratory Test Results
    25. Observation Class: Findings - Domain: Microbiology Specimen
    26. Observation Class: Findings - Domain: Microbiology Susceptibility
    27. Observation Class: Findings - Domain: Microscopic Findings
    28. Observation Class: Findings - Domain: Morphology
    29. Observation Class: Findings - Domain: Cardiovascular System Findings
    30. Observation Class: Findings - Domain: Musculoskeletal System Findings
    31. Observation Class: Findings - Domain: Nervous System Findings
    32. Observation Class: Findings - Domain: Ophthalmic Examinations
    33. Observation Class: Findings - Domain: Reproductive System Findings
    34. Observation Class: Findings - Domain: Respiratory System Findings
    35. Observation Class: Findings - Domain: Urinary System Findings
    36. Observation Class: Findings - Domain: Pharmacokinetics Concentrations
    37. Observation Class: Findings - Domain: Pharmacokinetics Parameters
    38. Observation Class: Findings - Domain: Physical Examination
    39. Observation Class: Findings - Domain: Functional Tests
    40. Observation Class: Findings - Domain: Questionnaires
    41. Observation Class: Findings - Domain: Disease Response and Clin Classification
    42. Observation Class: Findings - Domain: Subject Characteristics
    43. Observation Class: Findings - Domain: Subject Status
    44. Observation Class: Findings - Domain: Tumor/Lesion Identification
    45. Observation Class: Findings - Domain: Tumor/Lesion Results
    46. Observation Class: Findings - Domain: Vital Signs
    47. Observation Class: Findings - Domain: Findings About Events or Interventions
    48. Observation Class: Findings - Domain: Skin Response
    49. Observation Class: Trial Design - Domain: Trial Arms
    50. Observation Class: Trial Design - Domain: Trial Elements
    51. Observation Class: Trial Design - Domain: Trial Visits
    52. Observation Class: Trial Design - Domain: Trial Disease Assessments
    53. Observation Class: Trial Design - Domain: Trial Disease Milestones
    54. Observation Class: Trial Design - Domain: Trial Inclusion/Exclusion Criteria
    55. Observation Class: Trial Design - Domain: Trial Summary Information
    56. Observation Class: Relationships - Domain: Related Records
    57. Observation Class: Relationships - Domain: Supplemental Qualifiers for [domain name]
    58. Observation Class: Relationships - Domain: Related Subjects
    59. Observation Class: Study Reference - Domain: Non-host Organism Identifiers
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Related Records
RELREC (SDTMIG v3.3)
C147182 (NCIt V19.10d:)
C4687766 (UMLS CUI-1)
STUDYID
Item
Study Identifier
text
C2826693 (UMLS CUI [1])
STUDYID (SDTMIG 3.3)
C83082 (NCIt V19.10d)
Item
Related Domain Abbreviation
text
C0439849 (UMLS CUI [1,1])
C1883204 (UMLS CUI [1,2])
C0000723 (UMLS CUI [1,3])
RDOMAIN (SDTMIG 3.3)
C2826980 (NCIt V19.10d)
RDOMAIN
Code List
Related Domain Abbreviation
CL Item
Analysis Dataset (AD)
ADaM (Comment:en)
C1704642 (UMLS CUI-1)
C49563 (NCIt V19.10d)
CL Item
Adverse Events (AE)
C1705413 (UMLS CUI-1)
C49562 (NCIt V19.10d)
CL Item
Procedure Agents (AG)
C3888235 (UMLS CUI-1)
C117755 (NCIt V19.10d)
CL Item
Associated Persons Adverse Events (APAE)
SDTMIG-AP (Comment:en)
C4688600 (UMLS CUI-1)
C147168 (NCIt V19.10d)
CL Item
Associated Persons Biospecimen (APBS)
SDTMIG-AP (Comment:en)
C4687757 (UMLS CUI-1)
C147169 (NCIt V19.10d)
CL Item
Associated Persons Death Details (APDD)
SDTMIG-AP (Comment:en)
C4687758 (UMLS CUI-1)
C147170 (NCIt V19.10d)
CL Item
Associated Persons Demographics (APDM)
SDTMIG-AP (Comment:en)
C4329363 (UMLS CUI-1)
C132354 (NCIt V19.10d)
CL Item
Associated Persons Exposure (APEX)
SDTMIG-AP (Comment:en)
C4553046 (UMLS CUI-1)
C147171 (NCIt V19.10d)
CL Item
Associated Persons Laboratory Test Results (APLB)
SDTMIG-AP (Comment:en)
C4687759 (UMLS CUI-1)
C147172 (NCIt V19.10d)
CL Item
Associated Persons Medical History (APMH)
SDTMIG-AP (Comment:en)
C4687760 (UMLS CUI-1)
C147173 (NCIt V19.10d)
CL Item
Associated Persons Questionnaires (APQS)
SDTMIG-AP (Comment:en)
C4687761 (UMLS CUI-1)
C147174 (NCIt V19.10d)
CL Item
Relationship between Associated Persons and Subjects (APRELSUB)
SDTMIG-AP (Comment:en)
C4687762 (UMLS CUI-1)
C147175 (NCIt V19.10d)
CL Item
Associated Persons Reproductive System Findings (APRP)
SDTMIG-AP (Comment:en)
C4687763 (UMLS CUI-1)
C147176 (NCIt V19.10d)
CL Item
Associated Persons Subject Characteristics (APSC)
SDTMIG-AP (Comment:en)
C4553017 (UMLS CUI-1)
C147177 (NCIt V19.10d)
CL Item
Associated Persons Subject Status (APSS)
SDTMIG-AP (Comment:en)
C4553488 (UMLS CUI-1)
C147178 (NCIt V19.10d)
CL Item
Associated Persons Substance Use (APSU)
SDTMIG-AP (Comment:en)
C4687764 (UMLS CUI-1)
C147179 (NCIt V19.10d)
CL Item
Non-Compliant ADaM Dataset (AX)
ADaM (Comment:en)
C3714936 (UMLS CUI-1)
C111282 (NCIt V19.10d)
CL Item
Biospecimen Events (BE)
SDTMIG-PGx (Comment:en)
C3811654 (UMLS CUI-1)
C111138 (NCIt V19.10d)
CL Item
Biospecimen Findings (BS)
SDTMIG-PGx (Comment:en)
C3814390 (UMLS CUI-1)
C111137 (NCIt V19.10d)
CL Item
Clinical Events (CE)
C2827664 (UMLS CUI-1)
C85441 (NCIt V19.10d)
CL Item
Concomitant/Prior Medications (CM)
C1704627 (UMLS CUI-1)
C49568 (NCIt V19.10d)
CL Item
Comments (CO)
C1705247 (UMLS CUI-1)
C49569 (NCIt V19.10d)
CL Item
Cardiovascular System Findings (CV)
C3538987 (UMLS CUI-1)
C102605 (NCIt V19.10d)
CL Item
Drug Accountability (DA)
C1704643 (UMLS CUI-1)
C49578 (NCIt V19.10d)
CL Item
Death Details; Death Diagnosis and Details (DD)
C2986893 (UMLS CUI-1)
C95087 (NCIt V19.10d)
CL Item
Device Events (DE)
SDTMIG-MD (Comment:en)
C3541240 (UMLS CUI-1)
C102616 (NCIt V19.10d)
CL Item
Device Identifiers (DI)
SDTMIG-MD (Comment:en)
C3541881 (UMLS CUI-1)
C102618 (NCIt V19.10d)
CL Item
Demographics (DM)
C1704791 (UMLS CUI-1)
C49572 (NCIt V19.10d)
CL Item
Device Properties (DO)
SDTMIG-MD (Comment:en)
C3539061 (UMLS CUI-1)
C102619 (NCIt V19.10d)
CL Item
Device-Subject Relationships (DR)
SDTMIG-MD (Comment:en)
C3540849 (UMLS CUI-1)
C102620 (NCIt V19.10d)
CL Item
Disposition (DS)
C1705555 (UMLS CUI-1)
C49576 (NCIt V19.10d)
CL Item
Device Tracking and Disposition (DT)
SDTMIG-MD (Comment:en)
C3542920 (UMLS CUI-1)
C102621 (NCIt V19.10d)
CL Item
Device In-Use (DU)
SDTMIG-MD (Comment:en)
C3540681 (UMLS CUI-1)
C102622 (NCIt V19.10d)
CL Item
Protocol Deviations (DV)
C1704645 (UMLS CUI-1)
C49585 (NCIt V19.10d)
CL Item
Device Exposure (DX)
SDTMIG-MD (Comment:en)
C3538936 (UMLS CUI-1)
C102617 (NCIt V19.10d)
CL Item
Exposure as Collected (EC)
C3890233 (UMLS CUI-1)
C117466 (NCIt V19.10d)
CL Item
Endocrine System Findings (ED)
not defined in SDTMIG v3.3 (Comment:en)
C3538926 (UMLS CUI-1)
C102630 (NCIt V19.10d)
CL Item
ECG Test Results (EG)
C1705651 (UMLS CUI-1)
C49626 (NCIt V19.10d)
CL Item
Exposure (EX)
C1704625 (UMLS CUI-1)
C49587 (NCIt V19.10d)
CL Item
Findings About Events or Interventions (FA)
C2827665 (UMLS CUI-1)
C85442 (NCIt V19.10d)
CL Item
Functional Tests (FT)
C3890579 (UMLS CUI-1)
C117756 (NCIt V19.10d)
CL Item
Gastrointestinal System Findings (GI)
not defined in SDTMIG v3.3 (Comment:en)
C3539617 (UMLS CUI-1)
C102640 (NCIt V19.10d)
CL Item
Hematopoietic System Findings (HM)
not defined in SDTMIG v3.3 (Comment:en)
C3538713 (UMLS CUI-1)
C102641 (NCIt V19.10d)
CL Item
Healthcare Encounters (HO)
C3889614 (UMLS CUI-1)
C117757 (NCIt V19.10d)
CL Item
Inclusion/Exclusion Criteria Not Met (IE)
C1881173 (UMLS CUI-1)
C61536 (NCIt V19.10d)
CL Item
Immunogenicity Specimen Assessments (IS)
C3812801 (UMLS CUI-1)
C112320 (NCIt V19.10d)
CL Item
Laboratory Test Results (LB)
C1705214 (UMLS CUI-1)
C49592 (NCIt V19.10d)
CL Item
Microbiology Specimen (MB)
C1706181 (UMLS CUI-1)
C49602 (NCIt V19.10d)
CL Item
Medical History (MH)
C1704706 (UMLS CUI-1)
C49603 (NCIt V19.10d)
CL Item
Microscopic Findings (MI)
C2986901 (UMLS CUI-1)
C95095 (NCIt V19.10d)
CL Item
Musculoskeletal System Findings (MK)
C3539059 (UMLS CUI-1)
C102674 (NCIt V19.10d)
CL Item
Meal Data (ML)
C1706380 (UMLS CUI-1)
C49604 (NCIt V19.10d)
CL Item
Morphology (MO)
C3538743 (UMLS CUI-1)
C102671 (NCIt V19.10d)
CL Item
Microbiology Susceptibility (MS)
C1881819 (UMLS CUI-1)
C61531 (NCIt V19.10d)
CL Item
Nervous System Findings (NV)
C3540591 (UMLS CUI-1)
C102677 (NCIt V19.10d)
CL Item
Ophthalmic Examinations (OE)
C4552124 (UMLS CUI-1)
C147180 (NCIt V19.10d)
CL Item
Non-host Organism Identifiers (OI)
C5202881 (UMLS CUI-1)
C161329 (NCIt V19.10d)
CL Item
Pharmacogenomics Biomarker (PB)
SDTMIG-PGx (Comment:en)
C3819255 (UMLS CUI-1)
C106552 (NCIt V19.10d)
CL Item
Pharmacokinetics Concentrations (PC)
SDTMIG-PGx (Comment:en)
C1706367 (UMLS CUI-1)
C49606 (NCIt V19.10d)
CL Item
Physical Examination (PE)
C1744699 (UMLS CUI-1)
C49608 (NCIt V19.10d)
CL Item
Pharmacogenomics/Genetics Findings (PF)
SDTMIG-PGx (Comment:en)
C3815179 (UMLS CUI-1)
C111289 (NCIt V19.10d)
CL Item
Pharmacogenomics/Genetics Methods and Supporting Information (PG)
SDTMIG-PGx (Comment:en)
C1882354 (UMLS CUI-1)
C61529 (NCIt V19.10d)
CL Item
Pool Definition (POOLDEF)
SEND (Comment:en)
C4687765 (UMLS CUI-1)
C147181 (NCIt V19.10d)
CL Item
Pharmacokinetic Parameters (PP)
C1705911 (UMLS CUI-1)
C49607 (NCIt V19.10d)
CL Item
Procedures (PR)
C3538935 (UMLS CUI-1)
C102700 (NCIt V19.10d)
CL Item
Questionnaires (QS)
C1706422 (UMLS CUI-1)
C49609 (NCIt V19.10d)
CL Item
Respiratory System Findings (RE)
C2986904 (UMLS CUI-1)
C95098 (NCIt V19.10d)
CL Item
Related Records (RELREC)
C4687766 (UMLS CUI-1)
C147182 (NCIt V19.10d)
CL Item
Related Subjects (RELSUB)
C4552648 (UMLS CUI-1)
C147183 (NCIt V19.10d)
CL Item
Reproductive System Findings (RP)
C3541325 (UMLS CUI-1)
C102707 (NCIt V19.10d)
CL Item
Disease Response and Clin Classification (RS)
C3813325 (UMLS CUI-1)
C107097 (NCIt V19.10d)
CL Item
Subject Biomarker (SB)
SDTMIG-PGx (Comment:en)
C3811240 (UMLS CUI-1)
C106571 (NCIt V19.10d)
CL Item
Subject Characteristics (SC)
C1706465 (UMLS CUI-1)
C49610 (NCIt V19.10d)
CL Item
Subject Elements (SE)
C1705189 (UMLS CUI-1)
C49616 (NCIt V19.10d)
CL Item
Subject Disease Milestones (SM)
C4553627 (UMLS CUI-1)
C147184 (NCIt V19.10d)
CL Item
Skin Response (SR)
C3813610 (UMLS CUI-1)
C112420 (NCIt V19.10d)
CL Item
Subject Status (SS)
C3891295 (UMLS CUI-1)
C117655 (NCIt V19.10d)
CL Item
Substance Use (SU)
C1705534 (UMLS CUI-1)
C49615 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Adverse Events (SUPPAE)
C4687767 (UMLS CUI-1)
C147185 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Procedure Agents (SUPPAG)
C4687768 (UMLS CUI-1)
C147186 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Biospecimen Events (SUPPBE)
SDTMIG-PGx (Comment:en)
C4687769 (UMLS CUI-1)
C147187 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Biospecimen Findings (SUPPBS)
SDTMIG-PGx (Comment:en)
C4687770 (UMLS CUI-1)
C147189 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Clinical Events (SUPPCE)
C4687772 (UMLS CUI-1)
C147191 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Concomitant/Prior Medications (SUPPCM)
C4687774 (UMLS CUI-1)
C147193 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Cardiovascular System Findings (SUPPCV)
C4687776 (UMLS CUI-1)
C147195 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Drug Accountability (SUPPDA)
C4687777 (UMLS CUI-1)
C147196 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Death Details (human clinical trials) (SUPPDD)
C4687778 (UMLS CUI-1)
C147197 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Device Events (SUPPDE)
SDTMIG-MD (Comment:en)
C4687779 (UMLS CUI-1)
C147198 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Demographics (SUPPDM)
C4687781 (UMLS CUI-1)
C147200 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Device Properties (SUPPDO)
SDTMIG-MD (Comment:en)
C4687782 (UMLS CUI-1)
C147201 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Disposition (SUPPDS)
C4687784 (UMLS CUI-1)
C147203 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Device Tracking and Disposition (SUPPDT)
SDTMIG-MD (Comment:en)
C4687785 (UMLS CUI-1)
C147204 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Device In-Use (SUPPDU)
SDTMIG-MD (Comment:en)
C4687786 (UMLS CUI-1)
C147205 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Protocol Deviations (SUPPDV)
C4687787 (UMLS CUI-1)
C147206 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Device Exposure (SUPPDX)
SDTMIG-MD (Comment:en)
C4687788 (UMLS CUI-1)
C147207 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Exposure as Collected (SUPPEC)
C4687789 (UMLS CUI-1)
C147208 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for ECG Test Results (SUPPEG)
C4687790 (UMLS CUI-1)
C147209 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Environmental and Social Factors (SUPPER)
not defined in SDTMIG v3.3 (Comment:en)
C4554000 (UMLS CUI-1)
C147210 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Exposure (SUPPEX)
C4687791 (UMLS CUI-1)
C147211 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Findings About Events or Interventions (SUPPFA)
C4687792 (UMLS CUI-1)
C147212 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Healthcare Encounters (SUPPHO)
C4687796 (UMLS CUI-1)
C147216 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Inclusion/Exclusion Criteria Not Met (SUPPIE)
C4687798 (UMLS CUI-1)
C147218 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Immunogenicity Specimen Assessments (SUPPIS)
C4687799 (UMLS CUI-1)
C147219 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Laboratory Test Results (SUPPLB)
C4687800 (UMLS CUI-1)
C147220 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Microbiology Specimen (SUPPMB)
C4687802 (UMLS CUI-1)
C147222 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Medical History (SUPPMH)
C4687803 (UMLS CUI-1)
C147223 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Microscopic Findings (SUPPMI)
C4687804 (UMLS CUI-1)
C147224 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Musculoskeletal System Findings (SUPPMK)
C4687805 (UMLS CUI-1)
C147225 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Meal Data (SUPPML)
C4687806 (UMLS CUI-1)
C147226 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Microbiology Susceptibility (SUPPMS)
C4687807 (UMLS CUI-1)
C147227 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Nervous System Findings (SUPPNV)
C4687808 (UMLS CUI-1)
C147228 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Ophthalmic Examinations (SUPPOE)
C4687809 (UMLS CUI-1)
C147229 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Biomarker (SUPPPB)
SDTMIG-PGx (Comment:en)
C4687812 (UMLS CUI-1)
C147232 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Pharmacokinetics Concentrations (SUPPPC)
C4687813 (UMLS CUI-1)
C147233 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Physical Examination (SUPPPE)
C4687814 (UMLS CUI-1)
C147234 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Findings (SUPPPF)
SDTMIG-PGx (Comment:en)
C4687815 (UMLS CUI-1)
C147235 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Methods and Supporting Information (SUPPPG)
SDTMIG-PGx (Comment:en)
C4687816 (UMLS CUI-1)
C147236 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Pharmacokinetic Parameters (SUPPPP)
C4687818 (UMLS CUI-1)
C147238 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Procedures (SUPPPR)
C4687819 (UMLS CUI-1)
C147239 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Questionnaires (SUPPQS)
C4687820 (UMLS CUI-1)
C147240 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for ECG QT Correction Model Data (SUPPQT)
not defined in SDTMIG v3.3 (Comment:en)
C4687821 (UMLS CUI-1)
C147241 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Respiratory Test Results (SUPPRE)
C4687822 (UMLS CUI-1)
C147242 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Reproductive System Findings (SUPPRP)
C4687823 (UMLS CUI-1)
C147243 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Disease Response (SUPPRS)
C4687824 (UMLS CUI-1)
C147244 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Subject Biomarker (SUPPSB)
C4687825 (UMLS CUI-1)
C147245 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Subject Characteristics (SUPPSC)
C4687826 (UMLS CUI-1)
C147246 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Subject Disease Milestones (SUPPSM)
C4687829 (UMLS CUI-1)
C147249 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Skin Response (SUPPSR)
C4687830 (UMLS CUI-1)
C147250 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Subject Status (SUPPSS)
C4687831 (UMLS CUI-1)
C147251 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Substance Use (SUPPSU)
C4687832 (UMLS CUI-1)
C147252 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Tumor Response (SUPPTR)
C4687841 (UMLS CUI-1)
C147261 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Tumor/Lesion Identification (SUPPTU)
C4687844 (UMLS CUI-1)
C147264 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Urinary System Findings (SUPPUR)
C4687846 (UMLS CUI-1)
C147267 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Vital Signs (SUPPVS)
C4687847 (UMLS CUI-1)
C147268 (NCIt V19.10d)
CL Item
Supplemental Qualifiers for Whole Body Findings (SUPPWB)
not defined in SDTMIG v3.3 (Comment:en)
C4687848 (UMLS CUI-1)
C147269 (NCIt V19.10d)
CL Item
Subject Visits (SV)
C1704677 (UMLS CUI-1)
C49617 (NCIt V19.10d)
CL Item
Trial Arms (TA)
C1705538 (UMLS CUI-1)
C49618 (NCIt V19.10d)
CL Item
Trial Disease Assessments (TD)
C3889651 (UMLS CUI-1)
C117699 (NCIt V19.10d)
CL Item
Trial Elements (TE)
C1705540 (UMLS CUI-1)
C49619 (NCIt V19.10d)
CL Item
Trial Inclusion/Exclusion Criteria (TI)
C1704756 (UMLS CUI-1)
C49620 (NCIt V19.10d)
CL Item
Trial Disease Milestones (TM)
C4552802 (UMLS CUI-1)
C147270 (NCIt V19.10d)
CL Item
Tumor/Lesion Results (TR)
C3814152 (UMLS CUI-1)
C106578 (NCIt V19.10d)
CL Item
Trial Summary (TS)
C1704618 (UMLS CUI-1)
C53483 (NCIt V19.10d)
CL Item
Tumor/Lesion Identification (TU)
C3811255 (UMLS CUI-1)
C106577 (NCIt V19.10d)
CL Item
Trial Visits (TV)
C1704705 (UMLS CUI-1)
C49621 (NCIt V19.10d)
CL Item
Trial Sets (TX)
C2986909 (UMLS CUI-1)
C95103 (NCIt V19.10d)
CL Item
Urinary System Findings (UR)
C3541338 (UMLS CUI-1)
C102726 (NCIt V19.10d)
CL Item
Vital Signs (VS)
C1704629 (UMLS CUI-1)
C49622 (NCIt V19.10d)
USUBJID
Item
Unique Subject Identifier
text
C1710548 (UMLS CUI [1,1])
C2826693 (UMLS CUI [1,2])
USUBJID (SDTMIG 3.3)
C70731 (NCIt V19.10d)
IDVAR
Item
Identifying Variable
text
C0600091 (UMLS CUI [1,1])
C0439828 (UMLS CUI [1,2])
IDVAR (SDTMIG 3.3)
C83293 (NCIt V19.10d)
IDVARVAL
Item
Identifying Variable Value
text
C0600091 (UMLS CUI [1,1])
C0439828 (UMLS CUI [1,2])
IDVARVAL (SDTMIG 3.3)
C83294 (NCIt V19.10d)
Item
Relationship Type
text
C0439849 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
RELTYPE (SDTMIG 3.3)
C83393 (NCIt V19.10d)
RELTYPE
Code List
Relationship Type
CL Item
Many; Several (MANY)
C0439064 (UMLS CUI-1)
C78728 (NCIt V19.10d)
CL Item
ONE (ONE)
C0205447 (UMLS CUI-1)
C66832 (NCIt V19.10d)
RELID
Item
Relationship Identifier
text
C0439849 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
RELID (SDTMIG 3.3)
C83392 (NCIt V19.10d)
Back to the top of the page