CDISC CDASH Variable Terminology

Preferred Label : CDISC CDASH Variable Terminology;

NCIt synonyms : CDISC-CDASH VARIABLE;

NCIt definition : The terminology subset that includes terms relevant to the Clinical Data Interchange Standards Consortium (CDISC) variables used by the Clinical Data Acquisition Standards Harmonization (CDASH) group.;

Détails

Origin ID

C83188;

UMLS CUI

C2826786;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
subset_includes_concept
- Adverse Event Action Taken with Study Treatment [NCIt concept]
- Adverse Event Associated with Serious Medical Event [NCIt concept]
- Adverse Event Attribution to Product or Procedure [NCIt concept]
- Adverse Event Caused Study Discontinuation Indicator [NCIt concept]
- Adverse Event End Date [NCIt concept]
- Adverse Event End Time [NCIt concept]
- Adverse Event Occurrence [NCIt concept]
- Adverse Event Ongoing [NCIt concept]
- Adverse Event Outcome [NCIt concept]
- Adverse Event Seriousness Due to Congenital Anomaly [NCIt concept]
- Adverse Event Sponsor Defined Identifier [NCIt concept]
- Adverse Event Start Date [NCIt concept]
- Adverse Event Start Day [NCIt concept]
- Adverse Event Start Time [NCIt concept]
- Adverse Event Toxicity Grade [NCIt concept]
- Adverse Event Verbatim Description [NCIt concept]
- Adverse Event Yes No Indicator [NCIt concept]
- Adverse Event associated with Hospitalization [NCIt concept]
- Age [NCIt concept]
- Age Unit [NCIt concept]
- Birth Date [NCIt concept]
- Birth Day [NCIt concept]
- Birth Month [NCIt concept]
- Birth Time [NCIt concept]
- Birth Year [NCIt concept]
- Clinical Study Sponsor [NCIt concept]
- Clinical Trial Epoch [NCIt concept]
- Concomitant Agent [NCIt concept]
- Concomitant Medication Active Ingredient [NCIt concept]
- Concomitant Medication Administration Dose [NCIt concept]
- Concomitant Medication Adverse Event Number [NCIt concept]
- Concomitant Medication Daily Dose [NCIt concept]
- Concomitant Medication Dose Form [NCIt concept]
- Concomitant Medication Dose Frequency [NCIt concept]
- Concomitant Medication Dose Unit [NCIt concept]
- Concomitant Medication End Date [NCIt concept]
- Concomitant Medication End Time [NCIt concept]
- Concomitant Medication Medical History Number [NCIt concept]
- Concomitant Medication Ongoing [NCIt concept]
- Concomitant Medication Previous Occurrence [NCIt concept]
- Concomitant Medication Route of Administration [NCIt concept]
- Concomitant Medication Start Date [NCIt concept]
- Concomitant Medication Start Time [NCIt concept]
- Concomitant Medication Use Indication [NCIt concept]
- Concomitant Medication Use Occurrence [NCIt concept]
- Concomitant Medication Use Sponsor Defined Identifier [NCIt concept]
- Concomitant Medication Yes No Indicator [NCIt concept]
- Death Related to Adverse Event [NCIt concept]
- Demographics Date of Collection [NCIt concept]
- Disabling Adverse Event [NCIt concept]
- Disposition Continuation [NCIt concept]
- Disposition Dictionary Derived Term [NCIt concept]
- Disposition Start Date [NCIt concept]
- Disposition Start Time [NCIt concept]
- Drug Accountability Assessment Original Result [NCIt concept]
- Drug Accountability Assessment Result Original Units [NCIt concept]
- Drug Accountability Assessment Test [NCIt concept]
- Drug Accountability Date [NCIt concept]
- Drug Accountability Dispensed Treatment Label Identifier Reference [NCIt concept]
- Drug Accountability Performed [NCIt concept]
- Drug Accountability Record Categorization [NCIt concept]
- Drug Accountability Record Subcategorization [NCIt concept]
- Drug Accountability Returned Treatment Label Identifier Reference [NCIt concept]
- Drug Accountability Treatment Dispensation Date [NCIt concept]
- Drug Accountability Treatment Return Date [NCIt concept]
- Electrocardiogram Date [NCIt concept]
- Electrocardiogram Method [NCIt concept]
- Electrocardiogram Original Result [NCIt concept]
- Electrocardiogram Original Result Unit of Measure [NCIt concept]
- Electrocardiogram Performed [NCIt concept]
- Electrocardiogram Position [NCIt concept]
- Electrocardiogram Reference Identifier [NCIt concept]
- Electrocardiogram Results Clinically Significant Occurrence [NCIt concept]
- Electrocardiogram Test [NCIt concept]
- Electrocardiogram Time [NCIt concept]
- Electrocardiogram Time Point [NCIt concept]
- Ethnic Group [NCIt concept]
- Exposure Dose [NCIt concept]
- Exposure Dose Adjustment [NCIt concept]
- Exposure Dose Adjustment Reason [NCIt concept]
- Exposure Dose Description [NCIt concept]
- Exposure Dose Form [NCIt concept]
- Exposure Dose Frequency [NCIt concept]
- Exposure Dose Unit [NCIt concept]
- Exposure End Date [NCIt concept]
- Exposure End Time [NCIt concept]
- Exposure Flow Rate [NCIt concept]
- Exposure Flow Rate Unit of Measure [NCIt concept]
- Exposure Interruption Duration [NCIt concept]
- Exposure Interruption Duration Unit [NCIt concept]
- Exposure Location [NCIt concept]
- Exposure Lot Number [NCIt concept]
- Exposure Planned Dose [NCIt concept]
- Exposure Planned Dose Units [NCIt concept]
- Exposure Planned Occurrence [NCIt concept]
- Exposure Reference Identifier [NCIt concept]
- Exposure Reported Name of Treatment [NCIt concept]
- Exposure Route of Administration [NCIt concept]
- Exposure Start Date [NCIt concept]
- Exposure Start Time [NCIt concept]
- Exposure Time Point [NCIt concept]
- Exposure Total Volume Administration [NCIt concept]
- Exposure Total Volume Administration Unit [NCIt concept]
- Exposure Yes No Indicator [NCIt concept]
- Inclusion Exclusion Criteria Yes No Indicator [NCIt concept]
- Inclusion Exclusion Criterion Category [NCIt concept]
- Inclusion Exclusion Criterion Test [NCIt concept]
- Inclusion Exclusion Criterion Test Code [NCIt concept]
- Investigator Identifier [NCIt concept]
- Laboratory Test Category [NCIt concept]
- Laboratory Test Date [NCIt concept]
- Laboratory Test Name [NCIt concept]
- Laboratory Test Original Result [NCIt concept]
- Laboratory Test Original Result Unit [NCIt concept]
- Laboratory Test Performed [NCIt concept]
- Laboratory Test Protocol Test Conditions Occurrence [NCIt concept]
- Laboratory Test Reference Identifier [NCIt concept]
- Laboratory Test Reference Range Indicator [NCIt concept]
- Laboratory Test Reference Range Lower Limit Original Unit [NCIt concept]
- Laboratory Test Reference Range Upper Limit Original Unit [NCIt concept]
- Laboratory Test Reference Range for Character Results Standard Unit [NCIt concept]
- Laboratory Test Result Clinically Significant [NCIt concept]
- Laboratory Test Specimen Condition [NCIt concept]
- Laboratory Test Subcategory [NCIt concept]
- Laboratory Test Time [NCIt concept]
- Laboratory Test Time Point [NCIt concept]
- Life Threatening Adverse Event [NCIt concept]
- Medical History Category [NCIt concept]
- Medical History Completion Date [NCIt concept]
- Medical History Controlled [NCIt concept]
- Medical History End Date [NCIt concept]
- Medical History Occurrence [NCIt concept]
- Medical History Ongoing [NCIt concept]
- Medical History Reported Term [NCIt concept]
- Medical History Sponsor Defined Identifier [NCIt concept]
- Medical History Start Date [NCIt concept]
- Medical History Subcategory [NCIt concept]
- Medical History Yes No Indicator [NCIt concept]
- Next Trial Identification [NCIt concept]
- Other Actions taken in Response to Adverse Event [NCIt concept]
- Physical Exam Performed [NCIt concept]
- Physical Exam Yes No Indicator [NCIt concept]
- Physical Examination Abnormal Finding [NCIt concept]
- Physical Examination Clinically Significant [NCIt concept]
- Physical Examination Date [NCIt concept]
- Physical Examination Evaluator [NCIt concept]
- Physical Examination Finding [NCIt concept]
- Physical Examination Sponsor Defined Identifier [NCIt concept]
- Physical Examination Test [NCIt concept]
- Physical Examination Time [NCIt concept]
- Protocol Deviation [NCIt concept]
- Protocol Deviation Code [NCIt concept]
- Protocol Deviation Dictionary Derived Term [NCIt concept]
- Protocol Deviation End Date [NCIt concept]
- Protocol Deviation End Time [NCIt concept]
- Protocol Deviation Sponsor Defined Identifier [NCIt concept]
- Protocol Deviation Start Date [NCIt concept]
- Protocol Deviation Start Time [NCIt concept]
- Protocol Deviation Yes No Indicator [NCIt concept]
- Protocol Disposition Event [NCIt concept]
- Race [NCIt concept]
- Seriousness of Adverse Event [NCIt concept]
- Severity of Adverse Event [NCIt concept]
- Sex [NCIt concept]
- Site Unblinding Occurrence [NCIt concept]
- Study Identifier [NCIt concept]
- Study Site Identifier [NCIt concept]
- Study Site Number [NCIt concept]
- Study Treatment Course Completion Occurrence [NCIt concept]
- Subject Characteristic Performed [NCIt concept]
- Subject Characteristics Original Result [NCIt concept]
- Subject Characteristics Test [NCIt concept]
- Subject Characteristics Yes No Indicator [NCIt concept]
- Subject Identifier [NCIt concept]
- Substance Usage Start Date [NCIt concept]
- Substance Use Category [NCIt concept]
- Substance Use Dose Description [NCIt concept]
- Substance Use Dose Frequency [NCIt concept]
- Substance Use Dose Unit [NCIt concept]
- Substance Use Duration [NCIt concept]
- Substance Use Duration Units [NCIt concept]
- Substance Use End Date [NCIt concept]
- Substance Use Never Current Former [NCIt concept]
- Substance Use Reported Name [NCIt concept]
- Vendor Name [NCIt concept]
- Visit Date [NCIt concept]
- Visit End Date [NCIt concept]
- Visit Time [NCIt concept]
- Vital Signs Clinical Significance [NCIt concept]
- Vital Signs Completion Status [NCIt concept]
- Vital Signs Date [NCIt concept]
- Vital Signs Location [NCIt concept]
- Vital Signs Measurement [NCIt concept]
- Vital Signs Original Result [NCIt concept]
- Vital Signs Original Result Unit [NCIt concept]
- Vital Signs Performed [NCIt concept]
- Vital Signs Position [NCIt concept]
- Vital Signs Sponsor Defined Identifier [NCIt concept]
- Vital Signs Time [NCIt concept]
- Vital Signs Time Point [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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