Observation Class: Relationships - Domain: Related Records

  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

Similar models

Observation Class: Relationships - Domain: Related Records

  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)
Code List
Related Domain Abbreviation
CL Item
Analysis Dataset (AD)
ADaM (Comment:en)
CL Item
Adverse Events (AE)
(Comment:en)
CL Item
Procedure Agents (AG)
(Comment:en)
CL Item
Associated Persons Adverse Events (APAE)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Biospecimen (APBS)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Death Details (APDD)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Demographics (APDM)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Exposure (APEX)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Laboratory Test Results (APLB)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Medical History (APMH)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Questionnaires (APQS)
SDTMIG-AP (Comment:en)
CL Item
Relationship between Associated Persons and Subjects (APRELSUB)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Reproductive System Findings (APRP)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Subject Characteristics (APSC)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Subject Status (APSS)
SDTMIG-AP (Comment:en)
CL Item
Associated Persons Substance Use (APSU)
SDTMIG-AP (Comment:en)
CL Item
Non-Compliant ADaM Dataset (AX)
ADaM (Comment:en)
CL Item
Biospecimen Events (BE)
SDTMIG-PGx (Comment:en)
CL Item
Biospecimen Findings (BS)
SDTMIG-PGx (Comment:en)
CL Item
Clinical Events (CE)
(Comment:en)
CL Item
Concomitant/Prior Medications (CM)
(Comment:en)
CL Item
Comments (CO)
(Comment:en)
CL Item
Cardiovascular System Findings (CV)
(Comment:en)
CL Item
Drug Accountability (DA)
(Comment:en)
CL Item
Death Details; Death Diagnosis and Details (DD)
(Comment:en)
CL Item
Device Events (DE)
SDTMIG-MD (Comment:en)
CL Item
Device Identifiers (DI)
SDTMIG-MD (Comment:en)
CL Item
Demographics (DM)
(Comment:en)
CL Item
Device Properties (DO)
SDTMIG-MD (Comment:en)
CL Item
Device-Subject Relationships (DR)
SDTMIG-MD (Comment:en)
CL Item
Disposition (DS)
(Comment:en)
CL Item
Device Tracking and Disposition (DT)
SDTMIG-MD (Comment:en)
CL Item
Device In-Use (DU)
SDTMIG-MD (Comment:en)
CL Item
Protocol Deviations (DV)
(Comment:en)
CL Item
Device Exposure (DX)
SDTMIG-MD (Comment:en)
CL Item
Exposure as Collected (EC)
(Comment:en)
CL Item
Endocrine System Findings (ED)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
ECG Test Results (EG)
(Comment:en)
CL Item
Exposure (EX)
(Comment:en)
CL Item
Findings About Events or Interventions (FA)
(Comment:en)
CL Item
Functional Tests (FT)
(Comment:en)
CL Item
Gastrointestinal System Findings (GI)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
Hematopoietic System Findings (HM)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
Healthcare Encounters (HO)
(Comment:en)
CL Item
Inclusion/Exclusion Criteria Not Met (IE)
(Comment:en)
CL Item
Immunogenicity Specimen Assessments (IS)
(Comment:en)
CL Item
Laboratory Test Results (LB)
(Comment:en)
CL Item
Microbiology Specimen (MB)
(Comment:en)
CL Item
Medical History (MH)
(Comment:en)
CL Item
Microscopic Findings (MI)
(Comment:en)
CL Item
Musculoskeletal System Findings (MK)
(Comment:en)
CL Item
Meal Data (ML)
(Comment:en)
CL Item
Morphology (MO)
(Comment:en)
CL Item
Microbiology Susceptibility (MS)
(Comment:en)
CL Item
Nervous System Findings (NV)
(Comment:en)
CL Item
Ophthalmic Examinations (OE)
(Comment:en)
CL Item
Non-host Organism Identifiers (OI)
(Comment:en)
CL Item
Pharmacogenomics Biomarker (PB)
SDTMIG-PGx (Comment:en)
CL Item
Pharmacokinetics Concentrations (PC)
SDTMIG-PGx (Comment:en)
CL Item
Physical Examination (PE)
(Comment:en)
CL Item
Pharmacogenomics/Genetics Findings (PF)
SDTMIG-PGx (Comment:en)
CL Item
Pharmacogenomics/Genetics Methods and Supporting Information (PG)
SDTMIG-PGx (Comment:en)
CL Item
Pool Definition (POOLDEF)
SEND (Comment:en)
CL Item
Pharmacokinetic Parameters (PP)
(Comment:en)
CL Item
Procedures (PR)
(Comment:en)
CL Item
Questionnaires (QS)
(Comment:en)
CL Item
Respiratory System Findings (RE)
(Comment:en)
CL Item
Related Records (RELREC)
(Comment:en)
CL Item
Related Subjects (RELSUB)
(Comment:en)
CL Item
Reproductive System Findings (RP)
(Comment:en)
CL Item
Disease Response and Clin Classification (RS)
(Comment:en)
CL Item
Subject Biomarker (SB)
SDTMIG-PGx (Comment:en)
CL Item
Subject Characteristics (SC)
(Comment:en)
CL Item
Subject Elements (SE)
(Comment:en)
CL Item
Subject Disease Milestones (SM)
(Comment:en)
CL Item
Skin Response (SR)
(Comment:en)
CL Item
Subject Status (SS)
(Comment:en)
CL Item
Substance Use (SU)
(Comment:en)
CL Item
Supplemental Qualifiers for Adverse Events (SUPPAE)
(Comment:en)
CL Item
Supplemental Qualifiers for Procedure Agents (SUPPAG)
(Comment:en)
CL Item
Supplemental Qualifiers for Biospecimen Events (SUPPBE)
SDTMIG-PGx (Comment:en)
CL Item
Supplemental Qualifiers for Biospecimen Findings (SUPPBS)
SDTMIG-PGx (Comment:en)
CL Item
Supplemental Qualifiers for Clinical Events (SUPPCE)
(Comment:en)
CL Item
Supplemental Qualifiers for Concomitant/Prior Medications (SUPPCM)
(Comment:en)
CL Item
Supplemental Qualifiers for Cardiovascular System Findings (SUPPCV)
(Comment:en)
CL Item
Supplemental Qualifiers for Drug Accountability (SUPPDA)
(Comment:en)
CL Item
Supplemental Qualifiers for Death Details (human clinical trials) (SUPPDD)
(Comment:en)
CL Item
Supplemental Qualifiers for Device Events (SUPPDE)
SDTMIG-MD (Comment:en)
CL Item
Supplemental Qualifiers for Demographics (SUPPDM)
(Comment:en)
CL Item
Supplemental Qualifiers for Device Properties (SUPPDO)
SDTMIG-MD (Comment:en)
CL Item
Supplemental Qualifiers for Disposition (SUPPDS)
(Comment:en)
CL Item
Supplemental Qualifiers for Device Tracking and Disposition (SUPPDT)
SDTMIG-MD (Comment:en)
CL Item
Supplemental Qualifiers for Device In-Use (SUPPDU)
SDTMIG-MD (Comment:en)
CL Item
Supplemental Qualifiers for Protocol Deviations (SUPPDV)
(Comment:en)
CL Item
Supplemental Qualifiers for Device Exposure (SUPPDX)
SDTMIG-MD (Comment:en)
CL Item
Supplemental Qualifiers for Exposure as Collected (SUPPEC)
(Comment:en)
CL Item
Supplemental Qualifiers for ECG Test Results (SUPPEG)
(Comment:en)
CL Item
Supplemental Qualifiers for Environmental and Social Factors (SUPPER)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
Supplemental Qualifiers for Exposure (SUPPEX)
(Comment:en)
CL Item
Supplemental Qualifiers for Findings About Events or Interventions (SUPPFA)
(Comment:en)
CL Item
Supplemental Qualifiers for Healthcare Encounters (SUPPHO)
CL Item
Supplemental Qualifiers for Inclusion/Exclusion Criteria Not Met (SUPPIE)
CL Item
Supplemental Qualifiers for Immunogenicity Specimen Assessments (SUPPIS)
CL Item
Supplemental Qualifiers for Laboratory Test Results (SUPPLB)
CL Item
Supplemental Qualifiers for Microbiology Specimen (SUPPMB)
CL Item
Supplemental Qualifiers for Medical History (SUPPMH)
CL Item
Supplemental Qualifiers for Microscopic Findings (SUPPMI)
CL Item
Supplemental Qualifiers for Musculoskeletal System Findings (SUPPMK)
CL Item
Supplemental Qualifiers for Meal Data (SUPPML)
CL Item
Supplemental Qualifiers for Microbiology Susceptibility (SUPPMS)
CL Item
Supplemental Qualifiers for Nervous System Findings (SUPPNV)
(Comment:en)
CL Item
Supplemental Qualifiers for Ophthalmic Examinations (SUPPOE)
(Comment:en)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Biomarker (SUPPPB)
SDTMIG-PGx (Comment:en)
CL Item
Supplemental Qualifiers for Pharmacokinetics Concentrations (SUPPPC)
(Comment:en)
CL Item
Supplemental Qualifiers for Physical Examination (SUPPPE)
(Comment:en)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Findings (SUPPPF)
SDTMIG-PGx (Comment:en)
CL Item
Supplemental Qualifiers for Pharmacogenomics/Genetics Methods and Supporting Information (SUPPPG)
SDTMIG-PGx (Comment:en)
CL Item
Supplemental Qualifiers for Pharmacokinetic Parameters (SUPPPP)
(Comment:en)
CL Item
Supplemental Qualifiers for Procedures (SUPPPR)
(Comment:en)
CL Item
Supplemental Qualifiers for Questionnaires (SUPPQS)
(Comment:en)
CL Item
Supplemental Qualifiers for ECG QT Correction Model Data (SUPPQT)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
Supplemental Qualifiers for Respiratory Test Results (SUPPRE)
(Comment:en)
CL Item
Supplemental Qualifiers for Reproductive System Findings (SUPPRP)
(Comment:en)
CL Item
Supplemental Qualifiers for Disease Response (SUPPRS)
(Comment:en)
CL Item
Supplemental Qualifiers for Subject Biomarker (SUPPSB)
(Comment:en)
CL Item
Supplemental Qualifiers for Subject Characteristics (SUPPSC)
(Comment:en)
CL Item
Supplemental Qualifiers for Subject Disease Milestones (SUPPSM)
(Comment:en)
CL Item
Supplemental Qualifiers for Skin Response (SUPPSR)
(Comment:en)
CL Item
Supplemental Qualifiers for Subject Status (SUPPSS)
(Comment:en)
CL Item
Supplemental Qualifiers for Substance Use (SUPPSU)
(Comment:en)
CL Item
Supplemental Qualifiers for Tumor Response (SUPPTR)
(Comment:en)
CL Item
Supplemental Qualifiers for Tumor/Lesion Identification (SUPPTU)
(Comment:en)
CL Item
Supplemental Qualifiers for Urinary System Findings (SUPPUR)
(Comment:en)
CL Item
Supplemental Qualifiers for Vital Signs (SUPPVS)
(Comment:en)
CL Item
Supplemental Qualifiers for Whole Body Findings (SUPPWB)
not defined in SDTMIG v3.3 (Comment:en)
CL Item
Subject Visits (SV)
(Comment:en)
CL Item
Trial Arms (TA)
(Comment:en)
CL Item
Trial Disease Assessments (TD)
(Comment:en)
CL Item
Trial Elements (TE)
(Comment:en)
CL Item
Trial Inclusion/Exclusion Criteria (TI)
(Comment:en)
CL Item
Trial Disease Milestones (TM)
(Comment:en)
CL Item
Tumor/Lesion Results (TR)
(Comment:en)
CL Item
Trial Summary (TS)
(Comment:en)
CL Item
Tumor/Lesion Identification (TU)
(Comment:en)
CL Item
Trial Visits (TV)
(Comment:en)
CL Item
Trial Sets (TX)
(Comment:en)
CL Item
Urinary System Findings (UR)
(Comment:en)
CL Item
Vital Signs (VS)
(Comment:en)
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)
Code List
Relationship Type
CL Item
Many; Several (MANY)
CL Item
ONE (ONE)
RELID
Item
Relationship Identifier
text
C0439849 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
RELID (SDTMIG 3.3)
C83392 (NCIt V19.10d)