Information:
Error:
ID
38505
Description
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing; ODM derived from: https://clinicaltrials.gov/show/NCT01969370
Link
https://clinicaltrials.gov/show/NCT01969370
Keywords
Versions (1)
- 10/22/19 10/22/19 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
October 22, 2019
DOI
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License
Creative Commons BY 4.0
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Eligibility Cancer NCT01969370
Eligibility Cancer NCT01969370
- StudyEvent: Eligibility
Similar models
Eligibility Cancer NCT01969370
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Malignant Neoplasms
Item
cancer
boolean
C0006826 (UMLS CUI [1])
Disease length
Item
age of diagnosis
boolean
C0872146 (UMLS CUI [1])
Bilateral Carcinoma | Multiple malignancy
Item
presence of bilateral (or multiple) cancers
boolean
C1332549 (UMLS CUI [1])
C0346429 (UMLS CUI [2])
C0346429 (UMLS CUI [2])
Malignant Neoplasm Type Rare
Item
diagnosis of a rare type of cancer
boolean
C0006826 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0522498 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C0522498 (UMLS CUI [1,3])
Family history Details
Item
details of the family history
boolean
C0241889 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,2])
Condition Cardiovascular
Item
cardiovascular conditions
boolean
C0348080 (UMLS CUI [1,1])
C3887460 (UMLS CUI [1,2])
C3887460 (UMLS CUI [1,2])
Prolonged QT interval Electrocardiogram
Item
certain clinical findings, such as prolonged qt interval on electrocardiogram.
boolean
C0151878 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
C0013798 (UMLS CUI [1,2])
Hypertrophic Cardiomyopathy | Aortic Aneurysm
Item
presence of hypertrophic cardiomyopathy or aortic aneurysm
boolean
C0007194 (UMLS CUI [1])
C0003486 (UMLS CUI [2])
C0003486 (UMLS CUI [2])
Disease length
Item
age of diagnosis
boolean
C0872146 (UMLS CUI [1])
Family history
Item
presence of family history
boolean
C0241889 (UMLS CUI [1])
Neurodevelopmental Disorders Pediatric
Item
pediatric neurodevelopmental disorders
boolean
C1535926 (UMLS CUI [1,1])
C1521725 (UMLS CUI [1,2])
C1521725 (UMLS CUI [1,2])
Abnormality of brain morphology
Item
specific brain structural brain abnormalities
boolean
C4021085 (UMLS CUI [1])
Seizure Type
Item
presence of certain seizure types
boolean
C0036572 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
Dysmorphic features
Item
dysmorphic features
boolean
C0432072 (UMLS CUI [1])
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