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  1. Unified Medical Language System (UMLS) UMLS Quick Start Guide FAQs Customer Support UMLS Vocabularies A AIR ALT AOD AOT ATC B BI C CCC CCPSS CCS CCS_10 CCSR_10 ...
  2. Unified Medical Language System (UMLS) UMLS Quick Start Guide FAQs Customer Support UMLS Vocabularies A AIR ALT AOD AOT ATC B BI C CCC CCPSS CCS CCS_10 CCSR_10 ...
  3. Unified Medical Language System (UMLS) UMLS Quick Start Guide FAQs Customer Support UMLS Vocabularies A AIR ALT AOD AOT ATC B BI C CCC CCPSS CCS CCS_10 CCSR_10 ...
  4. ... NCI_CTRP. The source name is the same (Clinical Trials Reporting Program). National Drug File - Reference Terminology (NDF-RT) update: This is the final release ...
  5. ... for Adverse Events 3.0 CTCAE_5 Common Terminology Criteria for Adverse Events 5.0 CTEP-SDC Cancer Therapy Evaluation Program - Simple Disease Classification CTRP Clinical Trials Reporting Program DCP NCI Division of Cancer Prevention Program ...
  6. ... for Adverse Events 3.0 CTCAE_5 Common Terminology Criteria for Adverse Events 5.0 CTEP-SDC Cancer Therapy Evaluation Program - Simple Disease Classification CTRP Clinical Trials Reporting Program DCP NCI Division of Cancer Prevention Program ...
  7. ... Events 3.0) NCI2020_CTCAE_5_2002D (Common Terminology Criteria for Adverse Events 5.0) NCI2020_CTEP-SDC_2002D (Cancer Therapy Evaluation Program - Simple Disease Classification) NCI2020_CTRP_2002D (Clinical Trials Reporting Program) NCI2020_CareLex_2002D (Content Archive Resource Exchange ...
  8. ... vocabularies. One new source: MED-RT (Medication Reference Terminology) One new NCI sub-source: NCI_CTRP-SDC (NCI Clinical Trials Reporting Program) NDF-RT update: This release includes the final ...
  9. ... 0 NCI_CTCAE_5 2020AB ENG 0 Common Terminology Criteria for Adverse Events 4.3 Subset NCI_CTCAE 2020AB ENG 0 Cancer Therapy Evaluation Program - Simple Disease Classification NCI_CTEP-SDC 2020AB ENG 0 Clinical Trials Reporting Program Terms NCI_CTRP 2020AB ENG 0 Content ...
  10. ... NCI2020_CTCAE_3_2002D NCI_CTCAE_3 Common Terminology Criteria for Adverse Events 5.0, ... Trials Reporting Program, 2002D NCI2020_CTRP_2002D NCI_CTRP Content ...
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