Date of birth
Item
Date of birth
text
C0001779 (UMLS CUI [1])
Item
Gender
text
C0079399 (UMLS CUI [1])
Informed consent
Item
Informed consent
boolean
C0021430 (UMLS CUI [1])
Tobacco consume
Item
Tobacco consume
text
C0543414 (UMLS CUI [1])
Family history of coronary heart disease
Item
Family history of coronary heart disease
boolean
C0455404 (UMLS CUI [1])
Patient address
Item
Patient address
text
C0421449 (UMLS CUI [1])
Allergies
Item
Allergies
text
C0020517 (UMLS CUI [1])
Patient ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
First name
Item
First name
text
C1443235 (UMLS CUI [1])
Study Participation status
Item
Does patient participate in another study trial?
boolean
C2348568 (UMLS CUI [1])
Insurance
Item
Insurance
text
C0021672 (UMLS CUI [1])
Postal code
Item
Postal code
text
C0421454 (UMLS CUI [1])
Ethnic Group
Item
Patient Ethnicity
text
C0015031 (UMLS CUI [1])
Race
Item
Race
text
C0034510 (UMLS CUI [1])
Physician name
Item
Attending pysician name
text
C2361125 (UMLS CUI [1])
Telephone number
Item
Telephone number
text
C1515258 (UMLS CUI [1])
Reduced life expectancy
Item
Reduced life expectancy
boolean
C1858274 (UMLS CUI [1])
Allergy to contrast medium
Item
Allergy to contrast medium
boolean
C0570562 (UMLS CUI [1])
Occupation
Item
Occupation
text
C0028811 (UMLS CUI [1])
Hospitalization since previous visit
Item
Hospitalization since previous visit
boolean
C0019993 (UMLS CUI [1])
Premature termination of study
Item
Premature termination of study
boolean
C2348570 (UMLS CUI [1])
Primary physician
Item
Primary physician
text
C0017319 (UMLS CUI [1])
Admission source
Item
Admission source
text
C0553514 (UMLS CUI [1])
OPS-Codes
Item
OPS-Codes
text
C1550373 (UMLS CUI [1])