Quality of Life Questionnaire - Gastrointestinal Neuroendocrine Tumors 21 CDISC Protocol Terminology PQ/CMC Interpretation Code (numeric) Terminology PQ/CMC Specification Status Terminology CDISC Protocol Subject Allocation Response Terminology CDISC SEND Null Flavor Reason Terminology GDC Terminology Primary Site of Disease Cytogenetic Risk Group-CALGB Criteria for AML Restriction Endonuclease ICDC Terminology Normal or Tumor Sample Pathology Indicator PQ/CMC Strength Operator Terminology Read Pair Number First Variant Gene Symbol ICDC Value Terminology GDC Value Terminology Library Strand Sequenced Question Target Capture Kit Identifier ChIP-Seq Antibody Name Reflux Treatment Type Indicator ALL Medical History Table ALL Authorized Value Terminology SeroNet Research Participant Metadata SeroNet Prior Test Result SeroNet Assay Target Metadata SeroNet Assay Metadata SeroNet Authorized Values CRF1 Registration Table CRF2 History and Physical Exam at Diagnosis Table CRF2 History and Physical Exam Family Medical History Table CRF2 History and Physical Exam Initial History Table CRF2 History and Physical Exam Patient Medical History Table CRF3 Diagnosis Biopsy Table CRF3 Diagnosis CSF Table CRF3 Diagnosis CT Scan Table CRF3 Diagnosis MR Spectroscopy Table CRF3 Diagnosis MRI Brain Table CRF3 Diagnosis MRI Spine Table CRF3 Diagnosis PET Imaging Table CRF3 Diagnosis Re-Biopsy Table CRF4 Treatment Additional Surgeries Table CRF4 Treatment Chemotherapy Table CRF4 Treatment Complementary Table CRF4 Treatment Re-Irradiation Table CRF4 Treatment Radiation Table CRF4 Treatment Steroids during Re-Irradiation Table CRF4 Treatment Steroids during Radiation Table CRF4 Treatment Steroids Table CRF4 Treatment Surgery Table CRF4 Treatment Table CRF5 Response Evaluation Clinical Evaluation Table CRF5 Response Evaluation Image Evaluation Table CRF5 Response Evaluation Time Point Table CRF6 DIPG Imaging Assessment Morphology Table CRF6 DIPG Imaging Assessment Perfusion Table CRF6 DIPG Imaging Assessment Ratio Table CRF6 DIPG Imaging Assessment Signal Characteristics Table CRF6 DIPG Imaging Assessment Table CRF6 DMG Imaging Assessment Morphology Table CRF6 DMG Imaging Assessment MRS Table CRF6 DMG Imaging Assessment Perfusion Table CRF6 DMG Imaging Assessment Ratio Table CRF6 DMG Imaging Assessment Signal Characteristics Table CRF6 DMG Imaging Assessment Table CRF7 Pathology Review Immunohistochemistry Test Table CRF7 Pathology Review Table CRF8 Pathology Review Genomics Performed Table CRF8 Pathology Review Table CRF8 Pathology Review Targeted Genomics Table PQ/CMC Expiration Date Classification Terminology PQ/CMC Retest Date Classification Terminology HL Subject Response Table HL Authorized Value Terminology Personal Medical History Whole Genome Sequencing Read Depth PQ/CMC Release Profile Terminology CDISC SDTM Action Taken with Tobacco Product Terminology PRO-CTCAE Version 1.0 Questionnaire Terminology PRO-CTCAE Attribute Value Terminology CDISC SDTM Microbiology Susceptibility Test Standard Character Result Terminology International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Terminology ICH M11 Terminology ICH M11 Reason for Amendment Value Set Terminology ICH M11 Trial Blinding Role Value Set Terminology Disease or Disorder Missing Value Reason Not Applicable C1272460 Determination of a value is not relevant in the current context. (NCI) A report has been received but the description provided does not appear to relate to an adverse event. This code allows a report to be recorded for administration purposes, even if it doesn't meet the requirements for adverse event reporting. SeroNet Determination of a value is not relevant in the current context. {NA} ICH ICDC Does Not Apply DIPG/DMG C48660 CDISC Not applicable NOT APPLICABLE PRO-CTCAE Device Problem Code (Appendix B) Qualitative Concept FDA not applicable IMDRF:A25 PCDC Not Applicable No Apparent Adverse Event Not_Applicable GDC NA N/A {Not applicable} Not Applicable Determination of a value is not relevant in the current context. Not Applicable N/A No unit of measure required FDA Individual Case Safety Report Terminology CDRH Medical Device Problem Terminology Adverse Event Outcome ICSR Terminology Operator of Medical Device ICSR Terminology Occupation ICSR Terminology Location of Event Occurrence ICSR Terminology Clinical Data Interchange Standards Consortium Terminology CDISC SDTM Trial Phase Terminology CDISC SDTM Yes No Unknown or Not Applicable Response Terminology CDISC SDTM Action Taken with Study Treatment Terminology CDISC SDTM Terminology CDISC SEND Terminology