Patient code
Item
text
C1301894 (UMLS CUI [1])
Birth date
Item
date
C0421451 (UMLS CUI [1])
Item
integer
C0079399 (UMLS CUI [1])
CL Item
(1)
C0043210 (UMLS CUI-1)
(Comment:nl)
CL Item
(2)
C0025266 (UMLS CUI-1)
(Comment:nl)
Place of birth
Item
text
C0032040 (UMLS CUI [1])
Country of birth
Item
text
C1300001 (UMLS CUI [1])
Postcode at diagnosis
Item
text
C0421454 (UMLS CUI [1,1])
C4071762 (UMLS CUI [1,2])
Emigration date
Item
date
C0013975 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Death date / last contact date
Item
date
C1148348 (UMLS CUI [1,1])
C0805839 (UMLS CUI [1,2])
Vital status
Item
text
C1148433 (UMLS CUI [1])
Performance status
Item
text
C1518965 (UMLS CUI [1])
Comorbidity
Item
text
C0009488 (UMLS CUI [1])
Body height
Item
integer
C0005890 (UMLS CUI [1])
Body weight
Item
float
C0005910 (UMLS CUI [1])
Intoxications
Item
text
C0947848 (UMLS CUI [1])
Medical History
Item
text
C0262926 (UMLS CUI [1])
Pathology laboratory
Item
text
C0030664 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
Pathology ID
Item
text
C1299222 (UMLS CUI [1])
Diagnosis / treatment setting
Item
text
C3176918 (UMLS CUI [1])
Patient number
Item
text
C1830427 (UMLS CUI [1])
Specialty
Item
text
C0037778 (UMLS CUI [1])
Specialist
Item
text
C2348234 (UMLS CUI [1])
Tumor number
Item
text
C0006826 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Diagnosis date
Item
date
C2316983 (UMLS CUI [1])
Diagnosis type
Item
text
C1550351 (UMLS CUI [1])
Localization
Item
text
C0475264 (UMLS CUI [1])
Laterality
Item
text
C0925205 (UMLS CUI [1])
Morphology
Item
text
C0332437 (UMLS CUI [1])
Tumor stage
Item
text
C1300072 (UMLS CUI [1])
Tumor grading
Item
text
C0919553 (UMLS CUI [1])
Diagnosis description
Item
text
C0011900 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
Leukocytes
Item
float
C0023516 (UMLS CUI [1])
Persistent monocytosis
Item
text
C0085702 (UMLS CUI [1,1])
C0205322 (UMLS CUI [1,2])
Neutrophils
Item
float
C0027950 (UMLS CUI [1])
Blasts bone marrow
Item
float
C1982687 (UMLS CUI [1])
Blasts peripheral blood
Item
float
C0368761 (UMLS CUI [1,1])
C0229664 (UMLS CUI [1,2])
Hemoglobin
Item
float
C0019046 (UMLS CUI [1])
Platelets
Item
float
C0005821 (UMLS CUI [1])
evaluable on
Item
text
C1516986 (UMLS CUI [1])
Cellularity
Item
text
C1561532 (UMLS CUI [1])
Fibrosis
Item
text
C2355575 (UMLS CUI [1])
Dyserythropoiesis
Item
text
C0221143 (UMLS CUI [1])
Dysmegakaryopoiesis
Item
text
C3699665 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Dysgranulopoiesis
Item
text
C0302090 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Auer rods
Item
text
C0333828 (UMLS CUI [1])
Ringed sideroblasts
Item
text
C0432608 (UMLS CUI [1])
Ferritine
Item
float
C0015879 (UMLS CUI [1])
Cytogenetic abnormality
Item
text
C0008625 (UMLS CUI [1])
Cytogenetics method
Item
text
C0010802 (UMLS CUI [1,1])
C0871511 (UMLS CUI [1,2])
Molecular tests
Item
text
C1513380 (UMLS CUI [1])
Molecular abnormality
Item
text
C1521991 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
Therapy
Item
text
C0087111 (UMLS CUI [1])
wait / no treatment
Item
text
C1298659 (UMLS CUI [1])
reason for no treatment
Item
text
C0566251 (UMLS CUI [1,1])
C0746919 (UMLS CUI [1,2])
Item
Side effects of treatment
text
C0600688 (UMLS CUI [1])
Code List
Side effects of treatment
CL Item
Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated (Grade 1)
C1513302 (UMLS CUI-1)
(Comment:en)
CL Item
Moderate; minimal, local or noninvasive intervention indicated; limiting age-appropriate instrumental ADL (Grade 2)
C1513374 (UMLS CUI-1)
(Comment:en)
CL Item
Severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self care ADL (Grade 3)
C1519275 (UMLS CUI-1)
(Comment:en)
CL Item
Life-threatening consequences; urgent intervention indicated (Grade 4)
C3537125 (UMLS CUI-1)
(Comment:en)
CL Item
Death related to AE (Grade 5)
C1705232 (UMLS CUI-1)
(Comment:en)
Treatment response
Item
text
C0521982 (UMLS CUI [1])
Response date
Item
date
C1704632 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Diagnostic response assesment
Item
text
C0431080 (UMLS CUI [1,1])
C1704632 (UMLS CUI [1,2])
Trial participation
Item
text
C0008976 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
Chemotherapy regimen
Item
text
C0392920 (UMLS CUI [1])
Agent
Item
text
C0450442 (UMLS CUI [1])
Number of courses
Item
integer
C2045831 (UMLS CUI [1])
Drug dose
Item
text
C0678766 (UMLS CUI [1])
Regimen start date
Item
date
C1531783 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Regimen stop date
Item
date
C1531784 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Agent start date
Item
date
C1531783 (UMLS CUI [1,1])
C0450442 (UMLS CUI [1,2])
Agent stop date
Item
date
C1531784 (UMLS CUI [1,1])
C0450442 (UMLS CUI [1,2])
Regimen adjustment
Item
text
C0392920 (UMLS CUI [1,1])
C2826232 (UMLS CUI [1,2])
Agent adjustment
Item
text
C0450442 (UMLS CUI [1,1])
C2826232 (UMLS CUI [1,2])
Reason regimen adjustment
Item
text
C0392920 (UMLS CUI [1,1])
C1299575 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
Reason agent adjustment
Item
text
C2826286 (UMLS CUI [1])
Reason regimen stopped
Item
text
C0392920 (UMLS CUI [1,1])
C0850893 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Reason agent stopped
Item
text
C0450442 (UMLS CUI [1,1])
C0850893 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
allogeneic / autologous
Item
text
C2242529 (UMLS CUI [1,1])
C1831743 (UMLS CUI [1,2])
Myeloablative therapy
Item
text
C1513784 (UMLS CUI [1])
Peripheral blood / bone marrow
Item
text
C0229664 (UMLS CUI [1,1])
C0005953 (UMLS CUI [1,2])
Donor type
Item
text
C0348079 (UMLS CUI [1])