CDISC Root Variable Terminology

Preferred Label : CDISC Root Variable Terminology;

NCIt synonyms : CDISC-OBSCLS; CDISC Observation Class Terminology;

NCIt definition : The terminology subset that includes terms relevant to the Clinical Data Interchange Standards Consortium (CDISC) root variables.;

Details

Origin ID

C82590;

UMLS CUI

C2826317;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
subset_includes_concept
- Accepted Record Flag [NCIt concept]
- Accountable Party [NCIt concept]
- Accountable Party Identifier [NCIt concept]
- Action Taken with Device [NCIt concept]
- Action Taken with Study Treatment [NCIt concept]
- Active Ingredient [NCIt concept]
- Adverse Event Line Number [NCIt concept]
- Analysis Method [NCIt concept]
- Anchor Variable Name [NCIt concept]
- Associated Persons Domain [NCIt concept]
- Baseline Flag [NCIt concept]
- Biospecimen Condition [NCIt concept]
- Biospecimen Type [NCIt concept]
- Category [NCIt concept]
- Character Result or Finding in Standard Format [NCIt concept]
- Chronicity [NCIt concept]
- Clinical Trial Branch [NCIt concept]
- Code [NCIt concept]
- Collection Date Time [NCIt concept]
- Completion Status [NCIt concept]
- Congenital Abnormality [NCIt concept]
- Continue [NCIt concept]
- Daily Dose [NCIt concept]
- Data Value Code [NCIt concept]
- Death Relationship [NCIt concept]
- Derived Flag [NCIt concept]
- Directionality [NCIt concept]
- Discontinue [NCIt concept]
- Disease Controlled [NCIt concept]
- Dispensed Treatment Label Identifier Reference [NCIt concept]
- Distribution [NCIt concept]
- Dosage Form Unit [NCIt concept]
- Dose [NCIt concept]
- Dose Adjustment [NCIt concept]
- Dose Adjustment Reason [NCIt concept]
- Dose Description [NCIt concept]
- Dose Regimen [NCIt concept]
- Dose-Rate [NCIt concept]
- Dosing Days to Detection [NCIt concept]
- Drug Vehicle [NCIt concept]
- Duration of Use [NCIt concept]
- Element Order [NCIt concept]
- End Date [NCIt concept]
- End Relative to Reference Period [NCIt concept]
- End Relative to Reference Time Point [NCIt concept]
- End Rule [NCIt concept]
- End Time [NCIt concept]
- Evaluation Interval [NCIt concept]
- Evaluation Interval Text [NCIt concept]
- Evaluator [NCIt concept]
- Evaluator Identifier [NCIt concept]
- Event Occurrence Indicator [NCIt concept]
- Exclude from Statistics Indicator [NCIt concept]
- External Filename [NCIt concept]
- Fasting Status Indicator [NCIt concept]
- Flow Rate [NCIt concept]
- Flow Rate Unit [NCIt concept]
- High Test Reference Range [NCIt concept]
- Hospitalization or Prolongation of Existing Hospitalization Required [NCIt concept]
- Identifier [NCIt concept]
- Indication [NCIt concept]
- Interruption Duration [NCIt concept]
- Interruption Duration Unit [NCIt concept]
- LOINC Code [NCIt concept]
- Laboratory Vendor Name [NCIt concept]
- Laterality [NCIt concept]
- Level of Consciousness [NCIt concept]
- Life Threatening [NCIt concept]
- Link Group Identifier [NCIt concept]
- Location [NCIt concept]
- Lot Number [NCIt concept]
- Lower Limit of Quantitation [NCIt concept]
- Maximum Number of Actual Assessments [NCIt concept]
- Maximum Time Allowed in Planned Assessment Interval [NCIt concept]
- Measurement, Test or Examination Detail [NCIt concept]
- MedDRA Body System or Organ Class Code [NCIt concept]
- MedDRA High Level Group Term [NCIt concept]
- MedDRA High Level Group Term Code [NCIt concept]
- MedDRA High Level Term [NCIt concept]
- MedDRA High Level Term Code [NCIt concept]
- MedDRA Low Level Term [NCIt concept]
- MedDRA Low Level Term Code [NCIt concept]
- MedDRA Preferred Term Code [NCIt concept]
- MedDRA Primary System Organ Class Code [NCIt concept]
- MedDRA System Organ Class [NCIt concept]
- Medical History Line Number [NCIt concept]
- Minimum Time Allowed in Planned Assessment Interval [NCIt concept]
- Name of the Reference Terminology [NCIt concept]
- Never Current Former Classification [NCIt concept]
- Non-Study Treatment Relationship [NCIt concept]
- Normal Range Lower Limit Original Unit [NCIt concept]
- Observation End Date Time [NCIt concept]
- Observation Object [NCIt concept]
- Observation Result [NCIt concept]
- Observation Start Date Time [NCIt concept]
- Occurs with Overdose [NCIt concept]
- Offset [NCIt concept]
- Original Result Unit [NCIt concept]
- Original Result or Finding [NCIt concept]
- Other Action Taken [NCIt concept]
- Other Medically Important Serious Event [NCIt concept]
- Outcome Death [NCIt concept]
- Parameter [NCIt concept]
- Parameter Short Name [NCIt concept]
- Pattern of Event [NCIt concept]
- Persistent or Significant Disability or Incapacity [NCIt concept]
- Pharmaceutical Dosage Form [NCIt concept]
- Pharmaceutical Strength [NCIt concept]
- Pharmaceutical Strength Unit [NCIt concept]
- Planned Assessment Interval [NCIt concept]
- Planned Dose [NCIt concept]
- Planned Dose Unit [NCIt concept]
- Planned End of Assessment Interval [NCIt concept]
- Planned Occurrence [NCIt concept]
- Planned Start of Assessment Interval [NCIt concept]
- Planned Time Point Name [NCIt concept]
- Planned Time Point Number [NCIt concept]
- Population Parameter [NCIt concept]
- Portion or Totality [NCIt concept]
- Pre-specified [NCIt concept]
- Prior Medication Usage [NCIt concept]
- Protocol Test Conditions Met [NCIt concept]
- Reason for Exclusion from Statistics [NCIt concept]
- Record Link Identifier [NCIt concept]
- Record Mood [NCIt concept]
- Reference Date Time [NCIt concept]
- Reference End Time Point End [NCIt concept]
- Reference ID [NCIt concept]
- Reference Start Time Point [NCIt concept]
- Reference Time Point [NCIt concept]
- Related to Cancer [NCIt concept]
- Reported Event Term [NCIt concept]
- Result Category [NCIt concept]
- Returned Treatment Label Identifier Reference [NCIt concept]
- Route of Administration [NCIt concept]
- Run Identifier [NCIt concept]
- Sequence Number [NCIt concept]
- Sequence of Planned Assessment Schedule [NCIt concept]
- Serious Event [NCIt concept]
- Severity [NCIt concept]
- Sign or Symptom [NCIt concept]
- Sponsor Device Identifier [NCIt concept]
- Sponsor ID [NCIt concept]
- Standard Result Unit [NCIt concept]
- Start Date [NCIt concept]
- Start Relative to Reference Period [NCIt concept]
- Start Relative to Reference Time Point [NCIt concept]
- Start Rule [NCIt concept]
- Start Time [NCIt concept]
- Study Medication Completed [NCIt concept]
- Subcategory [NCIt concept]
- Subject Continuance [NCIt concept]
- Subject Pool Identifier [NCIt concept]
- Subject Unblinding [NCIt concept]
- Subsequent Trial Activity [NCIt concept]
- Test Code [NCIt concept]
- Test Date [NCIt concept]
- Test Method [NCIt concept]
- Test Name [NCIt concept]
- Test Occurrence [NCIt concept]
- Test Time [NCIt concept]
- Total Volume Administered Unit [NCIt concept]
- Toxicity [NCIt concept]
- Toxicity Grade [NCIt concept]
- Transition Rule [NCIt concept]
- Treatment Dispense Date [NCIt concept]
- Treatment Name [NCIt concept]
- Treatment Return Date [NCIt concept]
- Treatment Vehicle Amount [NCIt concept]
- Treatment Vehicle Amount Unit [NCIt concept]
- Unplanned Element Description [NCIt concept]
- Upper Limit of Quantitation [NCIt concept]
- Use Duration Unit [NCIt concept]
- Value Null Flavor [NCIt concept]
- Version [NCIt concept]
- Version of the Reference Terminology [NCIt concept]
- Volume Administered [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients