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Data Element Short NameData Element Long NameData Element Preferred Question TextData Element Preferred DefinitionData Element VersionData Element Context NameData Element Context VersionData Element Public IDData Element Workflow StatusData Element Registration StatusData Element Begin DateData Element SourceData Element Concept Public IDData Element Concept Short NameData Element Concept Long NameData Element Concept VersionData Element Concept Context NameData Element Concept Context VersionObject Class Public IDObject Class Long NameObject Class Short NameObject Class Context NameObject Class VersionObject Class Concept NameObject Class Concept CodeObject Class Concept Public IDObject Class Concept Definition SourceObject Class Concept EVS SourceObject Class Concept Primary FlagProperty Public IDProperty Long NameProperty Short NameProperty Context NameProperty VersionProperty Concept NameProperty Concept CodeProperty Concept Public IDProperty Concept Definition SourceProperty Concept EVS SourceProperty Concept Primary FlagValue Domain Public IDValue Domain Short NameValue Domain Long NameValue Domain VersionValue Domain Context NameValue Domain Context VersionValue Domain TypeValue Domain DatatypeValue Domain Min LengthValue Domain Max LengthValue Domain Min ValueValue Domain Max ValueValue Domain Decimal PlaceValue Domain FormatValue Domain Concept NameValue Domain Concept CodeValue Domain Concept Public IDValue Domain Concept Definition SourceValue Domain Concept EVS SourceValue Domain Concept Primary FlagRepresentation Public IDRepresentation Long NameRepresentation Short NameRepresentation Context NameRepresentation VersionRepresentation Concept NameRepresentation Concept CodeRepresentation Concept Public IDRepresentation Concept Definition SourceRepresentation Concept EVS SourceRepresentation Concept Primary FlagValid ValuesValue Meaning NameValue Meaning DescriptionValue Meaning ConceptsPV Begin DatePV End DateValue Meaning PublicIDValue Meaning VersionClassification Scheme Short NameClassification Scheme VersionClassification Scheme Context NameClassification Scheme Context VersionClassification Scheme Item NameClassification Scheme Item Type NameClassification Scheme Item Public IdClassification Scheme Item VersionData Element Alternate Name Context NameData Element Alternate Name Context VersionData Element Alternate Name Data Element Alternate Name TypeDocument Document NameDocument TypeDerivation TypeDerivation MethodDerivation RuleConcatenation CharacterDDE Public IDDDE Long NameDDE VersionDDE Workflow StatusDDE ContextDDE Display Order
INSTC_COMP_OBJ_NUMInstance Composite Object NumberInstance NumberNumeric value that identifies a composite object instance, as specified in a DICOM tag.1CIP2.312414574RELEASEDQualified2005-10-04DICOM:Digital Imaging and Communications in Medicine2413216IMAG_STDY_INSTImaging Study Instance1CIP2.312402958Medical ImagingC16831caBIG1Medical ImagingC168312224877NCINCI_CONCEPT_CODEYes2413214InstanceC48364caBIG1InstanceC483642413213NCINCI_CONCEPT_CODEYes2414572COMP_OBJ_INST_NUMComposite Object Instance Number1CIP2.31Non EnumeratedNUMBER642233101NumberC25337caBIG1NumberC253372202701Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1caBIGUSED_BYInstance NumberInstance NumberPreferred Question Text
NCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711
ADM_DX_CD_SEQAdmission Diagnosis Code SequenceAdmitting Diagnoses Code SequenceCoded sequence that conveys the admitting diagnosis (diagnoses).1CIP2.312413226RELEASEDQualified2005-10-02DICOM:Digital Imaging and Communications in Medicine2182492ADM_DXAdmission Diagnosis1CIP2.312429760AdmissionC25385caBIG1AdmissionC253852203585NCINCI_CONCEPT_CODEYes2239981DiagnosisC15220caBIG1DiagnosisC152202202734NCINCI_CONCEPT_CODEYes2413224ADM_DX_CD_SEQAdmission Diagnosis Code Sequence1CIP2.31Non EnumeratedCHARACTER502429761Sequence CodeC25673:C25162caBIG1SequenceC256732203798NCINCI_CONCEPT_CODENoNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1caBIGUSED_BYAdmitting Diagnoses Code SequenceAdmitting Diagnoses Code SequPreferred Question Text
CodeC251622203865Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711CIP2.309999943(0008,1084)DICOM_TAG
MED_IMAG_ROW_NUMMedical Image Row NumberRowsNumeric value to represent the number of rows in an image.1CIP2.312413332RELEASEDQualified2005-10-03DICOM:Digital Imaging and Communications in Medicine2413329MED_IMAG_ROWMedical Image Row1CIP2.312402958Medical ImagingC16831caBIG1Medical ImagingC168312224877NCINCI_CONCEPT_CODEYes2236682RowC43378caBIG1RowC433782236514NCINCI_CONCEPT_CODEYes2413330IMAG_ROW_NUMImage Row Number1CIP2.31Non EnumeratedNUMBER602233101NumberC25337caBIG1NumberC253372202701Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1caBIGUSED_BYRowsRowsPreferred Question Text
NCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711CIP2.309999943(0028,0010)DICOM_TAG
TTL_COLLM_MM_NUMTotal Collimation Width Millimeter NumberTotal Collimation WidthThe width of the total collimation (in mm) over the area of active x-ray detection. Note: This will be equal to the number of effective detector rows multiplied by single collimation width. Required if Frame Type (0008,9007) Value 1 of this frame is ORIGINAL. May be present otherwise. (Standard-based)1CIP2.312413390RELEASEDQualified2005-10-03DICOM:Digital Imaging and Communications in Medicine2413385TTL_COLLM_WDTHTotal Collimation Width1CIP2.312413383Total CollimationC25304:C25216caBIG1TotalC253042204938NCINCI_CONCEPT_CODENo2236636WidthC25345caBIG1WidthC253452203977NCINCI_CONCEPT_CODEYes2413386WDTH_MM_NUMWidth Millimeter Number1CIP2.31Non EnumeratedNUMBER412233101NumberC25337caBIG1NumberC253372202701Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1caBIGUSED_BYTotal Collimation WidthTotal Collimation WidthPreferred Question Text
CollimationC252162203886NCINCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711caBIG1Total Collimation WidthDICOM Attribute Name
DICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1(0018,9307)DICOM_TAG
IMG_TBL_FD_ROTN_NUMImage Table Feed Per Rotation NumberTable Feed per RotationThe distance in mm that the table moves in one second during the gathering of data that resulted in this frame. For CT: Required if Frame Type (0008,9007) Value 1 of this frame is ORIGINAL and Acquisition Type (0018,9302) is SPIRAL or CONSTANT_ANGLE. May be present otherwise if Frame Type (0008,9007) Value 1 of this frame is DERIVED and Acquisition Type (0018,9302) is SPIRAL or CONSTANT_ANGLE. [Standard-based]2caBIG12414549RELEASEDQualified2007-09-10DICOM:Digital Imaging and Communications in Medicine2679580IMG_TBL_FEED_PER_ROTImage Table Feed Per Rotation1caBIG12423453ImageC48179caBIG1ImageC481792422618NCINCI_CONCEPT_CODEYes2679569Table Feed Per RevolutionC48441:C69427:C65039:C48439caBIG1TableC484412413391NCINCI_CONCEPT_CODENo2679795ROTATION_MM_NUMRotation Number2caBIG1Non EnumeratedNUMBER802679794Revolution NumberC48439:C25337caBIG1RevolutionC484392413369NCINCI_CONCEPT_CODENoNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1Table Feed per RotationDICOM Attribute NameTable Feed per RotationTable Feed per RotationPreferred Question Text
FeedC694272677879NCINCI_CONCEPT_CODENoNumberC253372202701Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711caBIG1(0018,9310)DICOM_TAG
PerC650392679568NCI_CONCEPT_CODENoDICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1gov.nih.nci.ncia.domain.Image.tableFeedPerRotationUML Qualified Attr
RevolutionC484392413369NCINCI_CONCEPT_CODEYesDICOM1caBIG1For Review - NCIA DICOM CDEsGROUP_TYPE28128281caBIG1Image:tableFeedPerRotationUML Class:UML Attr
NCIA_Model3caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
NCIA_Model3caBIG1Silver Review Modified CDEsGROUP_TYPE28389211
NBIA5caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
PT_ETHNGRP_CATPatient Ethnic Group CategoryEthnicitythe patient's/participant's self declared ethnic origination, independent of racial origination, based on OMB approved categories.4.2CTEP2.312002440RELEASEDQualified2005-04-272014060PT_ETHNGRPPatient Ethnic Group1.1CTEP2.312177068PatientPatientCTEP1PatientC169602202778NCINCI_CONCEPT_CODEYes2222293Ethnic GroupC16564CTEP1Ethnic GroupC165642221860NCINCI_CONCEPT_CODEYes2016566ETHNGRP_CATEthnic Group Category5.1CTEP2.31EnumeratedCHARACTER7222433877CategoryC25372caBIG1CategoryC253722203876NCINCI_CONCEPT_CODEYesNot Hispanic or LatinoA person not meeting the definition for Hispanic or Latino.A person not meeting the definition for Hispanic or Latino.25671101Condition1DCP1Subclinical Neoplastic LesionsDISEASE_TYPE28125161caBIG1caBIGUSED_BYcheck one (U.S. only)1-COMMENTCOMMENT
Hispanic or LatinoA person of Mexican, Puerto Rican, Cuban, Central or South American or other Spanish culture or origin, regardless of race.A person of Mexican, Puerto Rican, Cuban, Central or South American or other Spanish culture or origin, regardless of race.25811761DISEASE2CTEP2.31Phase II Lung CancerDISEASE_TYPE28120171CDISC1CDISCUSED_BYPatient EthnicityCRF TextAlternate Question Text
UnknownCould not be determined or unsureCould not be determined or unsure2002-02-1125725771NCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221CDISC1ETHNICContext Short NameEthnicityEthnicityPreferred Question Text
Not reportedNot provided or availableNot provided or available2003-10-1625725781CATEGORY2CTEP2.31Common Terminology Criteria for Adverse Events v3.0CATEGORY_TYPE28120321NIDCR1NIDCRUSED_BYData element and all values comply with Clinical Data Update System (CDUS) v3.0 Release 2SourceDATA_ELEMENT_SOURCE
Potential CDEs for Reuse1NIDCR1PBRNGROUP_TYPE28120341CCR1ETHNIC_CATEGORIESC3D NameCDISC SDTM v3.1.1REFERENCE
Protocol Forms1NIDCR1DPBRNGROUP_TYPE28120281CCR1CCRUSED_BYPatient Ethnic Group CateogyCRFAlternate Question Text
Protocol Forms1NIDCR1PEARLGROUP_TYPE28120391NHLBI1NHLBIUSED_BYEthnicity:Ethnicity:Alternate Question Text
Protocol Forms1NIDCR1NIDCRGROUP_TYPE28120411CIP2.309999943CIPUSED_BY
Category1DCP1Protocol Deviation NotificationCase Report Form28120701SPOREs2.309999943SPOREsUSED_BY
DCEG1PS&CC1Prostate, Lung, Colorectal and Ovarian Cancer Screening TrialCATEGORY_TYPE28120801DCP1DCPUSED_BY
DCEG1PS&CC1CGEMSGROUP_TYPE28120781CTEP2.3099999432002440HISTORICAL_CDE_ID
DCEG1PS&CC1Baseline Questionnaire for Female Participants BQF3GROUP_TYPE28120811caBIG1edu.northwestern.radiology.AIM.Patient.ethnicGroupUML Qualified Attr
DCEG1PS&CC1Baseline Questionnaire for Male Participants BQM3GROUP_TYPE28120821NHLBI1key_ted_ethnicityNMDP_FN
Type of Category1NIDCR1RestorativeCATEGORY_TYPE28120861caBIG1Patient:ethnicGroupUML Class:UML Attr
Type of Category1NIDCR1PreventiveCATEGORY_TYPE28120851
Type of Category1NIDCR1Oral SurgeryCATEGORY_TYPE28120931
Condition1DCP1Budesonide Lung NodulesDISEASE_TYPE28121021
Condition1DCP1SAMe - Hepatitis C cirrhosisDISEASE_TYPE28121481
Condition1DCP1Pancreatic Mucinous NeoplasmsDISEASE_TYPE28121491
Condition1DCP1Prostate - LycopeneDISEASE_TYPE28121511
Condition1DCP1Barretts Esophagus - ASA-EsomeprazoleDISEASE_TYPE28121521
Condition1DCP1Bronchial Dysplasia - SulindacDISEASE_TYPE28121541
Condition1DCP1Sporadic Colorectal Neoplasia - AtrovastatinDISEASE_TYPE28121551
CATEGORY2CTEP2.31Breast Cancer DataMartCATEGORY_TYPE28121561
Condition1DCP1Melanoma Pathobiology - LovastatinDISEASE_TYPE28121571
Condition1DCP1Polyphenon E - Hormone Receptor-Negative Breast CancerDISEASE_TYPE28121741
Condition1DCP1Safety Study of Resiquimod for Atyical NeviDISEASE_TYPE28121771
DESK1DCP1E-Progress ReportCATEGORY_TYPE28121781
Condition1DCP1Tissue Effect of Finasteride - Prostate CancerDISEASE_TYPE28121821
Condition1DCP1Atrovastatin in Women at High Risk for Breast CancerDISEASE_TYPE28121831
Condition1DCP1Spectral Markers in ASADISEASE_TYPE28121841
Condition1DCP1Se-Methyl-Seleno-L-Cystein (MSC) in Adult MenDISEASE_TYPE28121881
Condition1DCP1Polyphenon E - Pre-prostatectomy Prostate CancerDISEASE_TYPE28121891
Condition1DCP1Acolbifene - High Risk for Breast CancerDISEASE_TYPE28121901
Condition1DCP1ALA PDT - Oral LeukoplakiaDISEASE_TYPE28121941
Condition1DCP1Phase II Resiquimod - Atypical NeviDISEASE_TYPE28121971
Condition1DCP1DIM - Prostate CancerDISEASE_TYPE28122021
Integrative Cancer Research1caBIG1Cancer Gene Data CurationGROUP_TYPE28122041
Condition1DCP1Aminolevulinic Acid - Barrett's EsophagusDISEASE_TYPE28122771
FBPP1NHLBI1FBPP Pooled Database CATEGORY_TYPE28122421
DISEASE2CTEP2.31Phase II Breast CancerDISEASE_TYPE28122451
Condition1DCP1Drug and Carcinogen Enzymes - ResveratrolDISEASE_TYPE28122581
Condition1DCP1Polyphenon E - Bladder CancerDISEASE_TYPE28125391
Condition1DCP19cUAB30DISEASE_TYPE28125511
Condition1DCP1EGF Receptor Signaling in ACFDISEASE_TYPE28125531
Submission and Reporting1CTEP2.31Clinical Data Update SystemCATEGORY_TYPE28124461
Submission and Reporting1CTEP2.31SubGroups/Treatment AssignmentCATEGORY_TYPE28126211
Submission and Reporting1CTEP2.31Breast Cancer Data MartCATEGORY_TYPE28126241
Submission and Reporting1CTEP2.31AdEERSCATEGORY_TYPE28123831
Submission and Reporting1CTEP2.31General Data SummaryCATEGORY_TYPE28126151
Submission and Reporting1CTEP2.31Patient Demographic ItemsCATEGORY_TYPE28126231
Submission and Reporting1CTEP2.31Patient Administrative ItemsCATEGORY_TYPE28126181
Submission and Reporting1CTEP2.31Patient Treatment by CourseCATEGORY_TYPE28126191
Submission and Reporting1CTEP2.31Common Terminology Criteria for Adverse Events v3.0CATEGORY_TYPE28120321
Clinical Trial Mgmt Systems1caBIG1CTMS C3D Adopter SitesGROUP_TYPE28126251
Clinical Trial Mgmt Systems1caBIG1Reporting RequirementsGROUP_TYPE28126081
Clinical Trial Mgmt Systems1caBIG1Summary 4GROUP_TYPE28126281
Condition1DCP1PK and Safety - Novel Retinoid (9cUAB30)TRIAL_TYPE_USAGE28127681
NCIA Collection1caBIG1LIDCCATEGORY_TYPE28127701
NCIA Collection1caBIG1Case-Study-SeriesGROUP_TYPE28128031
NCIA Collection1caBIG1Research CaseGROUP_TYPE28128051
Clinical Trial Mgmt Systems1caBIG1Albert Einstein Medical CenterGROUP_TYPE28125731
Clinical Trial Mgmt Systems1caBIG1AE_104_085GROUP_TYPE28128121
Clinical Trial Mgmt Systems1caBIG1Arizona Cancer CenterGROUP_TYPE28122051
Clinical Trial Mgmt Systems1caBIG1AZCC 0210GROUP_TYPE28125751
Clinical Trial Mgmt Systems1caBIG1OHSU_288GROUP_TYPE28128321
Clinical Trial Mgmt Systems1caBIG1Oregon Health & Sciences UniversityGROUP_TYPE28128311
Condition1DCP1Imiquimod for Atypical NeviDISEASE_TYPE28128361
Condition1DCP1Polyethylene Glycol - Colon CarcinogenesisTRIAL_TYPE_USAGE28128431
Clinical Trial Mgmt Systems1caBIG1U of Pa Cancer CenterGROUP_TYPE28127271
Clinical Trial Mgmt Systems1caBIG1UPCC 07403GROUP_TYPE28125741
Clinical Trial Mgmt Systems1caBIG1Lombardi Cancer CenterGROUP_TYPE28125711
Clinical Trial Mgmt Systems1caBIG1Lombardi 02452GROUP_TYPE28125841
Clinical Trial Mgmt Systems1caBIG1Lombardi 03058GROUP_TYPE28125851
Clinical Trial Mgmt Systems1caBIG1Lombardi 04251GROUP_TYPE28125861
Clinical Trial Mgmt Systems1caBIG1U Nebraska Med CenterGROUP_TYPE28127261
Clinical Trial Mgmt Systems1caBIG1UC IrvineGROUP_TYPE28117161
Clinical Trial Mgmt Systems1caBIG1DFMO/Sul Colon III UCI 02_06GROUP_TYPE28125771
Clinical Trial Mgmt Systems1caBIG1UCI 0404GROUP_TYPE28125781
Condition1DCP1Bronchial Dysplasia - Myo-InositolTRIAL_TYPE_USAGE28128761
Disease Relapse1NHLBI1Lymphoma RelapseCATEGORY_TYPE28129261
Disease Relapse1NHLBI1Aplastic Anemia RelapseCATEGORY_TYPE28129231
Disease Relapse1NHLBI1Chronic Myelogenous Leukemia RelapseCATEGORY_TYPE28129241
Disease Relapse1NHLBI1Fanconi Anemia RelapseCATEGORY_TYPE28129251
Disease Relapse1NHLBI1Solid Tumor RelapseCATEGORY_TYPE28129281
BCR1caBIG1org.tgen.BCRUML_PACKAGE_NAME28129321
Condition1DCP1Exp. PK Formulations of SR13668TRIAL_TYPE_USAGE28129491
Clinical Trial Mgmt Systems1caBIG1Northwestern UniversityGROUP_TYPE28126931
Clinical Trial Mgmt Systems1caBIG1NU 0943_011GROUP_TYPE28126951
ASCO1caBIG1Colon Adjuvant Treatment SummaryGROUP_TYPE28127091
ASCO1caBIG1Breast Cancer Adjuvant TreatmentGROUP_TYPE28127131
Clinical Trial Mgmt Systems1caBIG1Duke UniversityGROUP_TYPE28117151
Clinical Trial Mgmt Systems1caBIG1Duke 500GROUP_TYPE28125801
Clinical Trial Mgmt Systems1caBIG1DC_0205GROUP_TYPE28125811
Clinical Trial Mgmt Systems1caBIG1P1_CPT_BCNU_RDGROUP_TYPE28125821
Clinical Trial Mgmt Systems1caBIG1PanvecGROUP_TYPE28125831
Clinical Trial Mgmt Systems1caBIG1ThermoDox StudyGROUP_TYPE28127231
Clinical Trial Mgmt Systems1caBIG1EORTC SAE ReportGROUP_TYPE28127161
ONS1caBIG1Multisite Research StudyGROUP_TYPE28127281
Category1DCP1Adverse EventsGROUP_TYPE28127301
Clinical Trial Mgmt Systems1caBIG1U WashingtonGROUP_TYPE28127311
Clinical Trial Mgmt Systems1caBIG1FES StudyGROUP_TYPE28127321
Clinical Trial Mgmt Systems1caBIG1FMISO StudyGROUP_TYPE28127331
Condition1DCP13, 3-Diindolylmethane Cervical IntraepithelialTRIAL_TYPE_USAGE28127351
Condition1DCP1Transdermal 4-OHT vs oral TAM DCIS of the BreastTRIAL_TYPE_USAGE28127361
Clinical Trial Mgmt Systems1caBIG1UNMC 284-04GROUP_TYPE28129811
Condition1DCP1Pioglitazone - Oral LeukoplakiaDISEASE_TYPE28129981
Condition1DCP1Sulindac - Increased Risk of MelanomaDISEASE_TYPE28130021
AIM1caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
NMDP: CDEs to be Reviewed1NHLBI12000r1: Recipient Baseline DataCase Report Form29648721
Condition1DCP1Ursodeoxycholic Acid - Barrett's PatientsTRIAL_TYPE_USAGE28130431
Condition1DCP1Erlotinib - Lesions of LungCase Report Form28130641
Clinical Trial Mgmt Systems1caBIG1St. Joseph HospitalGROUP_TYPE28130541
Clinical Trial Mgmt Systems1caBIG1SJO_ERCC1_07035GROUP_TYPE28130901
Category1DCP1Case Report Forms Version 3Case Report Form29573721
Clinical Trial Mgmt Systems1caBIG1Mass General HospitalGROUP_TYPE28130971
Submission and Reporting1CTEP2.31RECISTCATEGORY_TYPE28311871
Condition1DCP1Letrozole - Breast CancerTRIAL_TYPE_USAGE28427681
Condition1DCP1Breast Sulindac DFMOTRIAL_TYPE_USAGE28596281
Data Standards1caBIG1Standard CRFsGROUP_TYPE28599631
ASCO1caBIG1Chemotherapy AdministrationGROUP_TYPE28614731
KNearestNeighbors1caBIG1org.cabig.icr.asbp.parameterUML_PACKAGE_NAME28130281
ASCO1caBIG1Lung CancerGROUP_TYPE28984821
Iloprost Trial1SPOREs2.31Iloprost 12079GROUP_TYPE29319521
Condition1DCP1Polyphenon E in Women w/ Modulation of Arachidonic AcidTRIAL_TYPE_USAGE29365181
Condition1DCP1MyoInositol Chemoprevention in Colitis-Assoc. DysplasiaTRIAL_TYPE_USAGE29791721
Tobacco Product Assess Consort1caBIG1TobPRAC QuestionnaireGROUP_TYPE29504821
Condition1DCP1Metformin Colorectal CancerTRIAL_TYPE_USAGE30187811
Condition1DCP1Resveratrol in Postmenopausal WomenTRIAL_TYPE_USAGE30187821
AIM 1.51.5caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
The Cancer Genome Atlas1caBIG1Phase II Data ElementsCATEGORY_TYPE130819131
Condition1DCP1MSC and L SeMet in Adult MenDISEASE_TYPE31102191
Condition1DCP1Cholecalciferol and GenisteinDISEASE_TYPE31141631
Condition1DCP1Pioglitazone - Lung Pre-Surgical NSCLCTRIAL_TYPE_USAGE31528201
All Candidates1caBIG1All BRIDG CandidatesGROUP_TYPE31808871
Condition1DCP1Vitamin D - Bioactivity in the SkinTRIAL_TYPE_USAGE31828781
Condition1DCP1Metformin - Pre-Prostatectomy Prostate CancerTRIAL_TYPE_USAGE31828791
CATEGORY2CIP2.31PATIENT CHARACTERIS*CATEGORY_TYPE28117671
CATEGORY2CTEP2.31Adverse EventsCATEGORY_TYPE28119511
CATEGORY2CTEP2.31Disease DescriptionCATEGORY_TYPE28119531
CATEGORY2CTEP2.31Eligibility CriteriaCATEGORY_TYPE28119541
CATEGORY2CTEP2.31Follow-upCATEGORY_TYPE28119551
CATEGORY2CTEP2.31LabsCATEGORY_TYPE28119571
CATEGORY2CTEP2.31Patient Char.CATEGORY_TYPE28119591
CATEGORY2CTEP2.31Patient DemographicsCATEGORY_TYPE28119601
CATEGORY2CTEP2.31Protocol/Admin.CATEGORY_TYPE28119611
CATEGORY2CTEP2.31ResponseCATEGORY_TYPE28119621
CATEGORY2CTEP2.31TreatmentCATEGORY_TYPE28119631
CATEGORY2CTEP2.31Tumor MarkersCATEGORY_TYPE28119641
USAGE2CTEP2.31CLINICAL CAREUSAGE_TYPE28117811
USAGE2CTEP2.31CLINICAL TRIALSUSAGE_TYPE28117821
CRF_DISEASE2.31CTEP2.31BladderDISEASE_TYPE28119071
CRF_DISEASE2.31CTEP2.31BreastDISEASE_TYPE28118311
CRF_DISEASE2.31CTEP2.31ColorectalDISEASE_TYPE28118711
CRF_DISEASE2.31CTEP2.31GynecologicDISEASE_TYPE28119081
CRF_DISEASE2.31CTEP2.31LeukemiaDISEASE_TYPE28119091
CRF_DISEASE2.31CTEP2.31LungDISEASE_TYPE28118321
CRF_DISEASE2.31CTEP2.31MelanomaDISEASE_TYPE28118351
CRF_DISEASE2.31CTEP2.31ProstateDISEASE_TYPE28119101
CRF_DISEASE2.31CTEP2.31Upper GIDISEASE_TYPE28119111
TTU2.31CTEP2.31ALL Prev UntreatedTRIAL_TYPE_USAGE28117831
TTU2.31CTEP2.31AML Prev UntreatedTRIAL_TYPE_USAGE28117841
TTU2.31CTEP2.31APL Prev UntreatedTRIAL_TYPE_USAGE28117861
TTU2.31CTEP2.31Adjuvant EsophagealTRIAL_TYPE_USAGE28117891
TTU2.31CTEP2.31Adjuvant GastricTRIAL_TYPE_USAGE28117901
TTU2.31CTEP2.31Advanced EsophagealTRIAL_TYPE_USAGE28117921
TTU2.31CTEP2.31Advanced GastricTRIAL_TYPE_USAGE28117931
TTU2.31CTEP2.31CLL Prev UntreatedTRIAL_TYPE_USAGE28117951
TTU2.31CTEP2.31CML Prev UntreatedTRIAL_TYPE_USAGE28117971
TTU2.31CTEP2.31HCL Prev UntreatedTRIAL_TYPE_USAGE28118021
TTU2.31CTEP2.31MDS Prev UntreatedTRIAL_TYPE_USAGE28118061
TTU2.31CTEP2.31NSCLC 2nd LineTRIAL_TYPE_USAGE28118101
TTU2.31CTEP2.31NSCLC AdvancedTRIAL_TYPE_USAGE28118111
TTU2.31CTEP2.31Primary CervicalTRIAL_TYPE_USAGE28118171
TTU2.31CTEP2.31Primary EndometrialTRIAL_TYPE_USAGE28118181
TTU2.31CTEP2.31Primary OvarianTRIAL_TYPE_USAGE28118191
TTU2.31CTEP2.31SCLC 2nd LineTRIAL_TYPE_USAGE28118211
TTU2.31CTEP2.31SCLC ExtensiveTRIAL_TYPE_USAGE28118221
TTU2.31CTEP2.31SCLC LimitedTRIAL_TYPE_USAGE28118231
TTU2.31CTEP2.31Unresect PancreaticTRIAL_TYPE_USAGE28118271
TTU2.31CTEP2.31Resect PancreaticTRIAL_TYPE_USAGE28118291
DISEASE2CTEP2.31LungDISEASE_TYPE28118321
CRF_TTU2.31CTEP2.31AdjuvantTRIAL_TYPE_USAGE28117881
CRF_TTU2.31CTEP2.31NSCLC StagesTRIAL_TYPE_USAGE28118121
CRF_TTU2.31CTEP2.31AdvancedTRIAL_TYPE_USAGE28117911
CRF_TTU2.31CTEP2.31Unresect PancreaticTRIAL_TYPE_USAGE28118271
DISEASE2CTEP2.31MelanomaDISEASE_TYPE28118351
CRF_TTU2.31CTEP2.31Recurr GynecologicTRIAL_TYPE_USAGE28118301
CRF_TTU2.31CTEP2.31AML Prev UntreatedTRIAL_TYPE_USAGE28117841
DISEASE2CTEP2.31ColorectalDISEASE_TYPE28118711
CRF_TTU2.31CTEP2.31NeuroblastomaTRIAL_TYPE_USAGE28118741
CRF_TTU2.31CTEP2.31PilotTRIAL_TYPE_USAGE28118731
TTU2.31CTEP2.31Adult STS NewTRIAL_TYPE_USAGE28118841
TTU2.31CTEP2.31Adult STS RecurrentTRIAL_TYPE_USAGE28118851
TTU2.31CTEP2.31Ped STS NewTRIAL_TYPE_USAGE28118861
CRF_DISEASE2.31CTEP2.31SarcomaDISEASE_TYPE28118831
DISEASE2CTEP2.31SarcomaDISEASE_TYPE28118831
Phase1CTEP2.31Phase IIPhase Type28118911
Phase1CTEP2.31Phase IIIPhase Type28118901
TTU2.31CTEP2.31Ped STS RecurrentTRIAL_TYPE_USAGE28118891
TTU2.31CTEP2.31Multiple MyelomaTRIAL_TYPE_USAGE28119041
TTU2.31CTEP2.31Primary AmyloidosisTRIAL_TYPE_USAGE28119051
TTU2.31CTEP2.31Waldenstrom MacroglTRIAL_TYPE_USAGE28119061
DISEASE2CTEP2.31BladderDISEASE_TYPE28119071
DISEASE2CTEP2.31BreastDISEASE_TYPE28118311
DISEASE2CTEP2.31GynecologicDISEASE_TYPE28119081
DISEASE2CTEP2.31LeukemiaDISEASE_TYPE28119091
DISEASE2CTEP2.31ProstateDISEASE_TYPE28119101
DISEASE2CTEP2.31Upper GIDISEASE_TYPE28119111
DISEASE2CTEP2.31Head and NeckDISEASE_TYPE28119121
DISEASE2CTEP2.31LymphomaDISEASE_TYPE28119131
TTU2.31CTEP2.31Adjuvant BreastTRIAL_TYPE_USAGE28119141
TTU2.31CTEP2.31Adjuvant ColorectalTRIAL_TYPE_USAGE28119151
TTU2.31CTEP2.31Localized ProstateTRIAL_TYPE_USAGE28119161
TTU2.31CTEP2.31Advanced BreastTRIAL_TYPE_USAGE28119171
TTU2.31CTEP2.31Advanced ColorectalTRIAL_TYPE_USAGE28119181
TTU2.31CTEP2.31Advanced MelanomaTRIAL_TYPE_USAGE28119191
TTU2.31CTEP2.31Non-local ProstateTRIAL_TYPE_USAGE28119201
TTU2.31CTEP2.31ALL Relapse/RefractTRIAL_TYPE_USAGE28119211
TTU2.31CTEP2.31AML Relapse/RefractTRIAL_TYPE_USAGE28119221
TTU2.31CTEP2.31APL Relapse/RefractTRIAL_TYPE_USAGE28119231
TTU2.31CTEP2.31CLL Relapse/RefractTRIAL_TYPE_USAGE28119241
TTU2.31CTEP2.31CML Relapse/RefractTRIAL_TYPE_USAGE28119251
TTU2.31CTEP2.31HCL Relapse/RefractTRIAL_TYPE_USAGE28119261
TTU2.31CTEP2.31Local-Reg MelanomaTRIAL_TYPE_USAGE28119271
TTU2.31CTEP2.31MDS Relapse/RefractTRIAL_TYPE_USAGE28119281
TTU2.31CTEP2.31Met/UrothelialTRIAL_TYPE_USAGE28119291
TTU2.31CTEP2.31Muscle Invasive BladTRIAL_TYPE_USAGE28119301
TTU2.31CTEP2.31NSCLC Stage I-IIITRIAL_TYPE_USAGE28119311
TTU2.31CTEP2.31Pathology BreastTRIAL_TYPE_USAGE28119321
TTU2.31CTEP2.31Pathology ColorectalTRIAL_TYPE_USAGE28119331
TTU2.31CTEP2.31Pathology GynTRIAL_TYPE_USAGE28119341
TTU2.31CTEP2.31Pathology LeukemiaTRIAL_TYPE_USAGE28119351
TTU2.31CTEP2.31Pathology LungTRIAL_TYPE_USAGE28119361
TTU2.31CTEP2.31Pathology ProstateTRIAL_TYPE_USAGE28119371
TTU2.31CTEP2.31Recurrent GynTRIAL_TYPE_USAGE28119381
TTU2.31CTEP2.31Superficial BladderTRIAL_TYPE_USAGE28119391
TTU2.31CTEP2.31Bone Sarcoma NewTRIAL_TYPE_USAGE28119401
TTU2.31CTEP2.31Bone Sarcoma RecurTRIAL_TYPE_USAGE28119411
TTU2.31CTEP2.31Curative Head/NeckTRIAL_TYPE_USAGE28119421
TTU2.31CTEP2.31Hodgkin's LymphomaTRIAL_TYPE_USAGE28119431
TTU2.31CTEP2.31NonHodgkins LymphomaTRIAL_TYPE_USAGE28119441
TTU2.31CTEP2.31Palliative Head/NeckTRIAL_TYPE_USAGE28119451
DISEASE2CTEP2.31BrainDISEASE_TYPE28119491
DISEASE2CTEP2.31Multiple MyelomaDISEASE_TYPE28119501
CRF_DISEASE2.31CTEP2.31Head and NeckDISEASE_TYPE28119121
TTU2.31CTEP2.31Primary Brain RecurrTRIAL_TYPE_USAGE28120141
CRF_TTU2.31CTEP2.31Primary Brain NewTRIAL_TYPE_USAGE28120131
TTU2.31CTEP2.31Primary Brain NewTRIAL_TYPE_USAGE28120131
CRF_DISEASE2.31CTEP2.31BrainDISEASE_TYPE28119491
TTU2.31CTEP2.31Metastatic BrainTRIAL_TYPE_USAGE28120151
CRF_DISEASE2.31CTEP2.31Multiple MyelomaDISEASE_TYPE28119501
CCR Implementation1CCR1C3PRUSAGE_TYPE28116751
CCR Implementation1CCR1C3DUSAGE_TYPE28116731
CRF_TTU2.31CTEP2.31Multiple MyelomaTRIAL_TYPE_USAGE28119041
C3D Domain1CCR1CTMSv3.12C3D28116901
C3D Domain1CCR1CTMSv3.02C3D28116861
Category1DCP1Case Report FormsCase Report Form28117341
CRF_TTU2.31CTEP2.31Advanced ColorectalTRIAL_TYPE_USAGE28119181
CRF_TTU2.31CTEP2.31Adjuvant BreastTRIAL_TYPE_USAGE28119141
CRF_TTU2.31CTEP2.31NSCLC Stage I-IIITRIAL_TYPE_USAGE28119311
CRF_TTU2.31CTEP2.31Recurrent GynTRIAL_TYPE_USAGE28119381
CRF_TTU2.31CTEP2.31Advanced BreastTRIAL_TYPE_USAGE28119171
CRF_TTU2.31CTEP2.31Adjuvant ColorectalTRIAL_TYPE_USAGE28119151
CRF_TTU2.31CTEP2.31AML Relapse/RefractTRIAL_TYPE_USAGE28119221
CRF_TTU2.31CTEP2.31Localized ProstateTRIAL_TYPE_USAGE28119161
CRF_TTU2.31CTEP2.31Non-local ProstateTRIAL_TYPE_USAGE28119201
CRF_TTU2.31CTEP2.31Met/UrothelialTRIAL_TYPE_USAGE28119291
CRF_TTU2.31CTEP2.31Advanced EsophagealTRIAL_TYPE_USAGE28117921
CRF_TTU2.31CTEP2.31Primary OvarianTRIAL_TYPE_USAGE28118191
CRF_TTU2.31CTEP2.31Advanced MelanomaTRIAL_TYPE_USAGE28119191
CRF_TTU2.31CTEP2.31Curative Head/NeckTRIAL_TYPE_USAGE28119421
CRF_TTU2.31CTEP2.31Superficial BladderTRIAL_TYPE_USAGE28119391
CRF_TTU2.31CTEP2.31Primary CervicalTRIAL_TYPE_USAGE28118171
CRF_TTU2.31CTEP2.31Resect PancreaticTRIAL_TYPE_USAGE28118291
CRF_TTU2.31CTEP2.31Adult STS NewTRIAL_TYPE_USAGE28118841
Category1DCP1SeriousAdverseEventsCATEGORY_TYPE28123251
LIDC1CIP2.31Research CaseUSAGE_TYPE28123281
Integrative Cancer Research1caBIG1Dir Chall Lung StudyGROUP_TYPE28123401
Demonstration Applications1caBIG1CIAFGROUP_TYPE28123411
Demonstration Applications1caBIG1FirebirdCase Report Form28123471
Demonstration Applications1caBIG1RembrandtCase Report Form28123491
Data Standards1caBIG1StandardGROUP_TYPE28123581
Condition1DCP1Barretts EsophagusDISEASE_TYPE28123641
C3D Domain1CCR1caBIGUSAGE_TYPE28123671
SAE Reporting1caBIG1SAE ReportingUSAGE_TYPE28123701
Condition1DCP1Bladder CancerDISEASE_TYPE28123771
CATEGORY2CTEP2.31AdEERSCATEGORY_TYPE28123831
Adverse Events1CIP2.31AE/SAE CDEsUSAGE_TYPE28123871
Condition1DCP1Oral LeukoplakiaDISEASE_TYPE28123881
CRF_DISEASE2.31CTEP2.31NOSDISEASE_TYPE28118641
Condition1DCP1Polyphenon E for Cervical CaDISEASE_TYPE28123991
Condition1DCP1Sulindac for Breast CancerDISEASE_TYPE28124151
CATEGORY2CTEP2.31Clinical Data Update SystemCATEGORY_TYPE28124461
In-class Examples1Training1Short ExamplesCATEGORY_TYPE28124861
C3D Adopter CDEs for Reuse1CCR1CTMS 3.12BCATEGORY_TYPE28124901
CDISC Codelists1CDISC1CodelistsGROUP_TYPE28121001
CRF_TTU2.31CTEP2.31Treatment trialsTRIAL_TYPE_USAGE28123911
Condition1DCP1Unconjugated Isoflavones in Women at High Risk for Breast CancerDISEASE_TYPE28125021
INSTNC_NUM_IDInstance Unique IdentifierInstance NumberNumeric value to identify a single image instance.1CIP2.312413280RELEASED2005-10-03DICOM:Digital Imaging and Communications in Medicine2413216IMAG_STDY_INSTImaging Study Instance1CIP2.312402958Medical ImagingC16831caBIG1Medical ImagingC168312224877NCINCI_CONCEPT_CODEYes2413214InstanceC48364caBIG1InstanceC483642413213NCINCI_CONCEPT_CODEYes2191273UIDUnique Identifier1SPOREs2.31Non EnumeratedCHARACTER1642405190IdentifierC25364caBIG1IdentifierC253642202473NCINCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221CIP2.309999943(0020,0013)DICOM_TAGInstance NumberInstance NumberPreferred Question Text
2639962v1.0:2542197v1.1Image Scan Options CodeScan OptionParameters of image scanning sequence. [Standard-based]2caBIG12182242RELEASED2006-11-15DICOM:Digital Imaging and Communications in Medicine26399622423453v1.0:2639960v1.0Image Scan Options1caBIG12423453ImageC48179caBIG1ImageC481792422618NCINCI_CONCEPT_CODEYes2639960Scan OptionsC17999:C25374caBIG1ScanC179992202631NCINCI_CONCEPT_CODENo25421972542197v1.1Scan Options Code1.1caBIG1EnumeratedCHARACTER2162542196Scan Options CodeC17999:C25374:C25162caBIG1ScanC179992202631NCINCI_CONCEPT_CODENoTOMOTomographyImaging by sections or sectioning.C380932006-11-1525819391NCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1Scan OptionsDICOM Attribute Name2006 DICOM Standard - Sections 3, 5 & 62006 DICOM StandardDATA_ELEMENT_SOURCE
OptionsC253742203938NCINCI_CONCEPT_CODEYesOptionsC253742203938NCINCI_CONCEPT_CODENoROTARotational AcquisitionAcquisition where the x-ray source moves angularly in relation to the patient.C692292006-11-1527975661NCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711caBIG1(0018,0022)DICOM_TAGScan OptionScan OptionPreferred Question Text
CodeC251622203865Source => Name: NCI, NCI_CONCEPT_CODEYesPERPhase Encode ReorderingPhase Encode Reordering2006-11-1425819111NCIA Collection1caBIG1LIDCCATEGORY_TYPE28127701caBIG1caBIGUSED_BY
RGRespitatory GatingRespitatory Gating2006-11-1425819151DICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1gov.nih.nci.ncia.domain.Image.scanOptionsUML Qualified Attr
CGCardiac GatingCardiac Gating2006-11-1425819161NCIA Collection1caBIG1Case-Study-SeriesGROUP_TYPE28128031caBIG1Image:scanOptionsUML Class:UML Attr
PPGPeripheral Pulse GatingPeripheral Pulse Gating2006-11-1425819171NCIA Collection1caBIG1SeriesGROUP_TYPE28128061
FCFlow CompensationFlow Compensation2006-11-1425819181NCIA_Model3caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
PFFPartial Fourier-FrequencyPartial Fourier-Frequency2006-11-1425819191NCIA_Model3caBIG1Silver Review Modified CDEsGROUP_TYPE28389211
PFPPartial Fourier-PhasePartial Fourier-Phase2006-11-1425819201NBIA5caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
SPSpatial PresaturationSpatial Presaturation2006-11-1425819211LIDC1CIP2.31SeriesUSAGE_TYPE28123301
FSFat SaturationFat Saturation2006-11-1425819221
EKGEKG Event TriggerThe Scan Option attribute identifies the EKG Event Trigger technique which was used during the acquisition of the image. DICOM PS3.3: C.8.7.1.1.42006-11-1425819231
PHYPhysiological Event TriggerPhysiological Event Trigger2006-11-1525819241
CHASEBolus ChasingThe Scan Option attribute identifies the Bolus Chasing technique which was used during the acquisition of the image.2006-11-1525819401
STEPSteppingThe Scan Option attribute identifies the Stepping technique which was used during the acquisition of the image.2006-11-1525819411
2553761v1.0:2191273v1.0Image Service-Object Pair Class Unique IdentifierSOP Class UIDUniquely identifies the union of a specific set of DIMSE Services and one related Information Object Definition (as specified by a Service Class Definition) which completely defines a precise context for communication of operations on such an object or notifications about its state.2caBIG12182362RELEASEDStandard2007-06-25DICOM:Digital Imaging and Communications in Medicine25537612423453v1.0:2553660v1.0Image Service-Object Pair Class Unique Identifier1CIP2.312423453ImageC48179caBIG1ImageC481792422618NCINCI_CONCEPT_CODEYes2553660Service-Object Pair Class Unique IdentifierC63426:C25346:C45282:C25364caBIG1Service-Object PairC634262553609NCINCI_CONCEPT_CODENo2191273UIDUnique Identifier1SPOREs2.31Non EnumeratedCHARACTER1642405190IdentifierC25364caBIG1IdentifierC253642202473NCINCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221CIP2.309999943ENGLISHCONTEXT NAME2008 DICOM Standard, PS 3.4-2008, paragraph 3.9 DICOM Service Class DefinitionsDICOM StandardREFERENCE
ClassC253462203880NCINCI_CONCEPT_CODENoNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711caBIG1SOP Class UIDDICOM Attribute NameSOP Class UIDSOP Class UIDPreferred Question Text
UniqueC452822231550NCINCI_CONCEPT_CODENoNCIA Collection1caBIG1LIDCCATEGORY_TYPE28127701caBIG1(0008,0016)DICOM_TAG
IdentifierC253642202473NCINCI_CONCEPT_CODEYesDICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1gov.nih.nci.ncia.domain.Image.sopClassUIDUML Qualified Attr
NCIA Collection1caBIG1Case-Study-SeriesGROUP_TYPE28128031caBIG1Image:sopClassUIDUML Class:UML Attr
NCIA Collection1caBIG1Slice PositionGROUP_TYPE28128071caBIG1edu.northwestern.radiology.AIM.Image.sopClassUIDUML Qualified Attr
DICOM1caBIG1For Review - NCIA DICOM CDEsGROUP_TYPE28128281CIP2.309999943CIPUSED_BY
NCIA_Model3caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
AIM1caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
NCIA_Model3caBIG1Silver Review Modified CDEsGROUP_TYPE28389211
Data Standards1caBIG1Imaging Data StandardsGROUP_TYPE28473741
NBIA5caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
AIM 2.02caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
AIM 1.51.5caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
AIM 3.03caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
LIDC1CIP2.31Slice PositionUSAGE_TYPE28123311
Data Standards1caBIG1StandardGROUP_TYPE28123581
FRAME_REF_UIDFrame of Reference Unique IdentifierFrame of Reference UIDUniquely identifies the frame of referencefor a Series. Each series shall have a single frame of Rederence UID. [Standard-based]2caBIG12182463DRAFT NEW2007-06-25DICOM:Digital Imaging and Communications in Medicine26475812647579v1.0:2231610v1.0Frame of Reference Unique Identifier1caBIG12647579Frame of ReferenceC48360caBIG1Frame of ReferenceC483602430547NCINCI_CONCEPT_CODEYes2231610Unique IdentifierC45282:C25364caBIG1UniqueC452822231550NCINCI_CONCEPT_CODENo2191273UIDUnique Identifier1SPOREs2.31Non EnumeratedCHARACTER1642405190IdentifierC25364caBIG1IdentifierC253642202473NCINCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221CIP2.309999943ENGLISHCONTEXT NAMEFrame of Reference UIDFrame of Reference UIDPreferred Question Text
IdentifierC253642202473NCINCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711CIP2.309999943Frame of Reference UID DICOM Attribute Name
DICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901CIP2.309999943(0020,0052)DICOM_TAG
DICOM1caBIG1For Review - NCIA DICOM CDEsGROUP_TYPE28128281
CLIN_TRL_SITE_NM_TXTClinical Trial Site Name 64 Character TextClinical Trial Site NameThe words which describe the surroundings in which a type of research study that tests how well new medical treatments or other interventions work in people. [Manually-curated]_LO: A 64-character string with leading or trailing spaces being non-significant; NO CONTROL characters. [Standard-based]2caBIG12413209RELEASEDQualified2007-06-25DICOM:Digital Imaging and Communications in Medicine2648241CLIN_TRIAL_SITE_NMClinical Trial Site Name1caBIG12813549Clinical Trial SiteC71104:C37901caBIG1Clinical TrialC711042735720NCINCI_CONCEPT_CODENo2222841NameC42614caBIG1NameC426142222821NCINCI_CONCEPT_CODEYes25841172584117v1.064 Character Text1caBIG1Non EnumeratedCHARACTER1642637360String TextC45253:C25704caBIG1StringC452532539471NCINCI_CONCEPT_CODENoNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221CIP2.309999943Clinical Trial Site NameDICOM Attribute NameClinical Trial Site NameClinical Trial Site NamePreferred Question Text
SiteC379012202394NCINCI_CONCEPT_CODEYesTextC257042203863Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711CIP2.309999943(0012,0031)DICOM_TAGSite NameDCP Document TextAlternate Question Text
DICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1gov.nih.nci.ncia.domain.ClinicalTrialSite.siteNameUML Qualified Attr
DICOM1caBIG1For Review - NCIA DICOM CDEsGROUP_TYPE28128281caBIG1ClinicalTrialSite:siteNameUML Class:UML Attr
NCIA_Model3caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
PRSN_ETHNICITY_TXTPerson Ethnicity 16 Character TextEthnic GroupA 16-character string to describe the ethnic group or race of patient.2caBIG12660032RELEASEDApplication2009-08-14DICOM:Digital Imaging and Communications in Medicine25342882236731v1.0:2388843v1.0Person Ethnicity1caBIG12236731PersonC25190caBIG1PersonC251902202486NCINCI_CONCEPT_CODEYes2388843EthnicityC16564caBIG1Ethnic GroupC165642221860NCINCI_CONCEPT_CODEYes258411616_CHAR_TXT16 Character Text1caBIG1Non EnumeratedCHARACTER162637360String TextC45253:C25704caBIG1StringC452532539471NCINCI_CONCEPT_CODENoNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221caBIG1gov.nih.nci.ncia.domain.Person.ethnicGroupUML Qualified AttrEthnic GroupEthnic GroupPreferred Question Text
TextC257042203863Source => Name: NCI, NCI_CONCEPT_CODEYesNCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711caBIG1Person:ethnicGroupUML Class:UML Attr
NCIA Collection1caBIG1LIDCCATEGORY_TYPE28127701caBIG1gov.nih.nci.ncia.domain.Patient.ethnicGroupUML Qualified Attr
DICOM1caBIG1DICOM Tag CDEsCATEGORY_TYPE28127901caBIG1Patient:ethnicGroupUML Class:UML Attr
NCIA Collection1caBIG1Case-Study-SeriesGROUP_TYPE28128031caBIG1(0010,2160)DICOM_TAG
NCIA Collection1caBIG1Research CaseGROUP_TYPE28128051caBIG1Ethnic GroupDICOM Attribute Name
DICOM1caBIG1For Review - NCIA DICOM CDEsGROUP_TYPE28128281caBIG1edu.northwestern.radiology.AIM.Person.ethnicGroupUML Qualified Attr
NCIA_Model3caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
NCIA_Model3caBIG1Silver Review Modified CDEsGROUP_TYPE28389211
NBIA5caBIG1gov.nih.nci.ncia.domainUML_PACKAGE_NAME28125271
AIM 2.02caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
AIM 3.03caBIG1edu.northwestern.radiology.AIMUML_PACKAGE_NAME28130121
LIDC1CIP2.31Case-Study-SeriesUSAGE_TYPE28123381
LIDC1CIP2.31Research CaseUSAGE_TYPE28123281
BDY_WT_KGBody Weight in KilogramsBody Wt (Kg)Measurement of an individual's weight in kilograms.3CCR12003303RELEASEDQualified2002-07-092012400BDY_WTBody Weight3CCR12177197BodyBodyCCR1BodyC130412202687NCINCI_CONCEPT_CODEYes2177330WeightWeightCTEP1WeightC252082202868NCINCI_CONCEPT_CODEYes2018368WT_MSRMTWeight Measurement1CTEP2.31Non EnumeratedNUMBER1622184312MeasurementC25209caBIG1MeasurementC252092203848NCINCI_CONCEPT_CODEYesNCIA Projects1CIP2.31Rider ProjectCATEGORY_TYPE28120221SPOREs2.309999943BDY_WT_KGUSED_BYBody Wt (Kg)Body Wt (Kg)Preferred Question Text
Clinical Trial Mgmt Systems1caBIG1CTMS C3D Adopter SitesGROUP_TYPE28126251CIP2.309999943CIPUSED_BYBody Weight in KilogramsCRF TEXT2Alternate Question Text
NCIA Collection1caBIG1RIDERCATEGORY_TYPE28127711CIP2.309999943gov.nih.nci.ncia.domain.GeneralSeries.patientWeightUML Qualified AttrWeight (kg)CRF TEXT3Alternate Question Text
Clinical Trial Mgmt Systems1caBIG1Albert Einstein Medical CenterGROUP_TYPE28125731CIP2.309999943GeneralSeries:patientWeightUML Class:UML AttrWeightCRF TEXT5Alternate Question Text
Clinical Trial Mgmt Systems1caBIG1AE_104_085GROUP_TYPE28128121CIP2.309999943(0010,1030)DICOM_TAGBody WeightCRF TEXT6Alternate Question Text
Clinical Trial Mgmt Systems1caBIG1OHSU_288GROUP_TYPE28128321CCR1WEIGHT_KGC3D Name
Clinical Trial Mgmt Systems1caBIG1Oregon Health & Sciences UniversityGROUP_TYPE28128311caBIG1BDY_WT_KGUSED_BY
Clinical Trial Mgmt Systems1caBIG1U of Pa Cancer CenterGROUP_TYPE28127271CIP2.309999943BDY_WT_KGUSED_BY
Clinical Trial Mgmt Systems1caBIG1UPCC 07403GROUP_TYPE28125741
Clinical Trial Mgmt Systems1caBIG1Lombardi Cancer CenterGROUP_TYPE28125711
Clinical Trial Mgmt Systems1caBIG1Lombardi 02452GROUP_TYPE28125841
Clinical Trial Mgmt Systems1caBIG1Lombardi 03058GROUP_TYPE28125851
Clinical Trial Mgmt Systems1caBIG1Lombardi 04251GROUP_TYPE28125861
Clinical Trial Mgmt Systems1caBIG1U Nebraska Med CenterGROUP_TYPE28127261
Clinical Trial Mgmt Systems1caBIG1UC IrvineGROUP_TYPE28117161
Clinical Trial Mgmt Systems1caBIG1UCI 0404GROUP_TYPE28125781
Clinical Trial Mgmt Systems1caBIG1Northwestern UniversityGROUP_TYPE28126931
Clinical Trial Mgmt Systems1caBIG1NU 0943_011GROUP_TYPE28126951
Clinical Trial Mgmt Systems1caBIG1Duke UniversityGROUP_TYPE28117151
Clinical Trial Mgmt Systems1caBIG1DC_0205GROUP_TYPE28125811
Clinical Trial Mgmt Systems1caBIG1PanvecGROUP_TYPE28125831
Clinical Trial Mgmt Systems1caBIG1UNMC 284-04GROUP_TYPE28129811