Informazione:
Errore:
ID
41505
Descrizione
DELCODE is conducted by DZNE, the German Center for Neurodegenerative Diseases within the Helmholtz Association. The following information was taken from https://www.dzne.de/en/research/studies/clinical-studies/delcode/. Background and aims: One of the important aims of research into Alzheimer's is to find ways of detecting the disease early – if at all possible, as soon as the first minor symptoms appear, or even before any symptoms at all have appeared. Such detection capabilities are the necessary basis for development of therapies that can be applied at such early stages in the disease. Recent research indicates that such therapies could be more effective than therapies initiated during the disease's later stages. Over a period of several years, the DELCODE study is studying persons in early stages of the disease, along with various risk groups. The research is aimed at the development of procedures for characterizing early stages of the disease, at improving prediction of the course of the disease and at identifying new markers for early diagnosis of Alzheimer's-related dementia. Overview: DELCODE is set up to run for an initial period of three years, and to include a total of 1,000 study participants, who will be examined on a yearly basis. The group of participants will include persons with no complaints (healthy control subjects), patients with slight memory impairment or mild dementia and first-degree relatives of patients with diagnosed Alzheimer's disease. The minimum age for participants is 60. Course of the study: The examinations in the framework of the study will include a comprehensive interview carried out by a study investigator, a detailed neuropsychological examination (testing of memory functions and other areas of cognitive performance), a blood test and a cranial MRI scan. Optionally, subject to the study participant's consent in each case, a lumbar puncture (collection of cerebrospinal fluid) will be carried out." For more information (e.g. principle investigator and study coordination), please visit the above link or https://www.dzne.de. This document contains information about the PET investigation. The PET investigation form is for patients eligible for the PET sub-study of DELCODE only. Two PET investigations are to be conducted: a baseline investigation once eligible and a follow-up investigation 24 months after the baseline PET.
collegamento
https://www.dzne.de/en/research/studies/clinical-studies/delcode/
Keywords
versioni (1)
- 30/10/20 30/10/20 -
Titolare del copyright
DZNE (German Center for Neurodegenerative Diseases)
Caricato su
30 ottobre 2020
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 4.0
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DELCODE: DZNE – Longitudinal Cognitive Impairment and Dementia Study
Similar models
PET Investigation
- StudyEvent: ODM
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Study ID
Item
Studien ID
text
C2826693 (UMLS CUI [1])
Date of visit
Item
Visitendatum
date
C1320303 (UMLS CUI [1])
Item
PET‐Untersuchungszeitpunkt:
integer
C0439547 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
CL Item
Baseline‐PET (P0) (1)
CL Item
Follow‐Up‐PET nach 24 Monaten (P24) (2)
FBB-PET
Item
FBB-PET
boolean
C3818757 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
Date of investigation
Item
Datum des Untersuchungstags
date
C0011008 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
Time of investigation
Item
Untersuchungszeitpunkt
text
C1442880 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
PET investigation successfully performed
Item
Wurde die PET-Untersuchung erfolgreich durchgeführt?
boolean
C3258067 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
Sick proband / Proband didn't appear
Item
Proband krank / nicht erschienen
boolean
C2010702 (UMLS CUI [1])
C1548414 (UMLS CUI [2])
C1548414 (UMLS CUI [2])
Informed Consent missing
Item
Fehlende Einwilligung durch Proband/in
boolean
C0021430 (UMLS CUI [1,1])
C1705492 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,2])
Scanner or tracer not available
Item
Scanner oder Tracer nicht verfügbar
boolean
C5208732 (UMLS CUI [1,1])
C0686905 (UMLS CUI [1,2])
C0182349 (UMLS CUI [2,1])
C0686905 (UMLS CUI [2,2])
C0686905 (UMLS CUI [1,2])
C0182349 (UMLS CUI [2,1])
C0686905 (UMLS CUI [2,2])
Scanner malfunction after injection
Item
Scanner-Ausfall nach Injektion
boolean
C0182349 (UMLS CUI [1,1])
C1881681 (UMLS CUI [1,2])
C1548614 (UMLS CUI [1,3])
C1272883 (UMLS CUI [1,4])
C1881681 (UMLS CUI [1,2])
C1548614 (UMLS CUI [1,3])
C1272883 (UMLS CUI [1,4])
Loss of data after scan
Item
Datenverlust nach Scan
boolean
C1880251 (UMLS CUI [1,1])
C1548614 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C1548614 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
Other reasons for failure
Item
Sonstige
boolean
C3840932 (UMLS CUI [1,1])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
Name reasons
Item
Bitte Gründe benennen
text
C3840932 (UMLS CUI [1,1])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Injection of radiopharmaceutical
Item
Wurde das Radiopharmazeutikum injiziert?
boolean
C1272883 (UMLS CUI [1,1])
C0182638 (UMLS CUI [1,2])
C0182638 (UMLS CUI [1,2])
Informed consent signed
Item
Komplett unterschriebene studienspezifische Probandeneinwilligung für PET-Studie vorhanden?
boolean
C0021430 (UMLS CUI [1,1])
C0742766 (UMLS CUI [1,2])
C0742766 (UMLS CUI [1,2])
CL Item
Der DZNE-Zuweiser hat die Einwilligungserklärung bereits erhoben, und eine Kopie an die Nuklearmedizin gesandt (1)
CL Item
Die Einwilligungserklärung wurde von Ärzt/innen der Nuklearmedizin eingeholt (2)
PET - exclusion criteria examined daily
Item
PET-Ausschlusskriterien tagesaktuell geprüft?
boolean
C0032743 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
Item
PET-Ausschlusskriterien
integer
C0680251 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
CL Item
DZNE-PET-Kontraindikationsbogen (Regelfall bei BfS-pflichtigen Probanden) (1)
CL Item
Kliniküblicher Patienteneinwilligungsbogen (Regelfall bei klinisch rechtfertigender Indikation) (2)
MRI exclusion criteria examined (only PET-MRI)
Item
MRT-Ausschlusskriterien tagesaktuell geprüft? (nur bei PET-MRT)
boolean
C3641326 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
Item
MRT-Ausschlusskriterien
integer
C3641326 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
CL Item
DZNE-MRT-Kontraindikationsbogen (1)
CL Item
Kliniküblicher MRT-Patienteneinwilligungsbogen (2)
Item
Medikamenteneinnahme am Untersuchungstag
integer
C0013227 (UMLS CUI [1,1])
C1512806 (UMLS CUI [1,2])
C2584899 (UMLS CUI [1,3])
C1512806 (UMLS CUI [1,2])
C2584899 (UMLS CUI [1,3])
CL Item
Keine (0)
CL Item
Ja (1)
Pharmaceutical preparation
Item
Arzneimittel
text
C0013227 (UMLS CUI [1])
Injected dose
Item
Injizierte Dosis (berechnet)
float
C2986768 (UMLS CUI [1])
Exceeding of permitted maximum dose for FBB scans
Item
Hat die injizierte Aktivität die BfS-genehmigte Maximaldosis für FBB-Scans überschritten?
boolean
C2986768 (UMLS CUI [1,1])
C4296997 (UMLS CUI [1,2])
C0752079 (UMLS CUI [1,3])
C0032743 (UMLS CUI [1,4])
C3818757 (UMLS CUI [1,5])
C4296997 (UMLS CUI [1,2])
C0752079 (UMLS CUI [1,3])
C0032743 (UMLS CUI [1,4])
C3818757 (UMLS CUI [1,5])
Total Dose-Length-Product (only PET-CT)
Item
Gesamt Dosis-Längen-Produkt (DLP) (nur bei PET-CT)
float
C0439810 (UMLS CUI [1,1])
C3539930 (UMLS CUI [1,2])
C1699633 (UMLS CUI [1,3])
C3539930 (UMLS CUI [1,2])
C1699633 (UMLS CUI [1,3])
Medical abnormalities or other special incidents during or after the investigation
Item
Medizinische Auffälligkeiten oder andere besondere Vorkommnisse während oder nach der Untersuchung?
boolean
C0205476 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
Medical abnormalities or other special incidents during or after the investigation - specification
Item
Welche?
text
C0205476 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
Serious Adverse Events immediately reported
Item
(Serious) Adverse Events umgehend gemeldet? (Adverse Event Reporting Form des Herstellers) (nur für DELCODE relevant)
boolean
C1519255 (UMLS CUI [1,1])
C0205548 (UMLS CUI [1,2])
C4319718 (UMLS CUI [1,3])
C0205548 (UMLS CUI [1,2])
C4319718 (UMLS CUI [1,3])
Evidence of clinical abnormalities in transmission or emission
Item
Hinweise auf nicht studienbezogene klinische Auffälligkeiten in Transmission oder Emission?
boolean
C0332120 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
Evidence of not study-related clinical abnormalities in transmission or emission - specification
Item
Welche?
text
C0332120 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
Notes
Item
Anmerkungen
text
C0947611 (UMLS CUI [1])
FDG-PET
Item
FDG-PET
boolean
C3641247 (UMLS CUI [1])
Date of investigation - FDG-PET
Item
Datum des Untersuchungstags
date
C3641247 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Point in time of investigation - FDG-PET
Item
Untersuchungszeitpunkt
text
C3641247 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
C1442880 (UMLS CUI [1,2])
FDG-PET investigation successfully performed
Item
Wurde die PET-Untersuchung erfolgreich durchgeführt?
boolean
C3258067 (UMLS CUI [1,1])
C3641247 (UMLS CUI [1,2])
C3641247 (UMLS CUI [1,2])
Sick proband / Proband didn't appear
Item
Proband krank / nicht erschienen
boolean
C2010702 (UMLS CUI [1])
C1548414 (UMLS CUI [2])
C1548414 (UMLS CUI [2])
Informed Consent missing
Item
Fehlende Einwilligung durch Proband/in
boolean
C0021430 (UMLS CUI [1,1])
C1705492 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,2])
Scanner or Tracer not available
Item
Scanner oder Tracer nicht verfügbar
boolean
C5208732 (UMLS CUI [1,1])
C1706613 (UMLS CUI [1,2])
C3641247 (UMLS CUI [2,1])
C1706613 (UMLS CUI [2,2])
C1706613 (UMLS CUI [1,2])
C3641247 (UMLS CUI [2,1])
C1706613 (UMLS CUI [2,2])
Hyperglycemia
Item
Blutzuckerspiegel über Grenzwert
boolean
C0020456 (UMLS CUI [1])
Scanner malfunction after injection
Item
Scanner-Ausfall nach Injektion
text
C3641247 (UMLS CUI [1,1])
C1881681 (UMLS CUI [1,2])
C1548614 (UMLS CUI [1,3])
C1272883 (UMLS CUI [1,4])
C1881681 (UMLS CUI [1,2])
C1548614 (UMLS CUI [1,3])
C1272883 (UMLS CUI [1,4])
Loss of data after scan
Item
Datenverlust nach Scan
boolean
C1880251 (UMLS CUI [1,1])
C1548614 (UMLS CUI [1,2])
C3641247 (UMLS CUI [1,3])
C1548614 (UMLS CUI [1,2])
C3641247 (UMLS CUI [1,3])
Other reasons for failure
Item
Sonstige
boolean
C3840932 (UMLS CUI [1,1])
C5200924 (UMLS CUI [1,2])
C3641247 (UMLS CUI [1,3])
C5200924 (UMLS CUI [1,2])
C3641247 (UMLS CUI [1,3])
Name reasons
Item
Bitte Gründe benennen
text
C3840932 (UMLS CUI [1,1])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C5200924 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Injection of radiopharmaceutical
Item
Wurde das Radiopharmazeutikum injiziert?
boolean
C1272883 (UMLS CUI [1,1])
C0182638 (UMLS CUI [1,2])
C0182638 (UMLS CUI [1,2])
Informed consent signed
Item
Komplett unterschriebene studienspezifische Probandeneinwilligung für PET-Studie vorhanden?
boolean
C0021430 (UMLS CUI [1,1])
C0742766 (UMLS CUI [1,2])
C0742766 (UMLS CUI [1,2])
CL Item
Der DZNE-Zuweiser hat die Einwilligungserklärung bereits erhoben, und eine Kopie an die Nuklearmedizin gesandt (1)
CL Item
Die Einwilligungserklärung wurde von Ärzt/innen der Nuklearmedizin eingeholt (2)
PET - exclusion criteria examined daily
Item
PET-Ausschlusskriterien tagesaktuell geprüft?
boolean
C0032743 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
Item
PET-Ausschlusskriterien
integer
C0680251 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0032743 (UMLS CUI [1,2])
CL Item
DZNE-PET-Kontraindikationsbogen (Regelfall bei BfS-pflichtigen Probanden) (1)
CL Item
Kliniküblicher Patienteneinwilligungsbogen (Regelfall bei klinisch rechtfertigender Indikation) (2)
MRI exclusion criteria examined (only PET-MRI)
Item
MRT-Ausschlusskriterien tagesaktuell geprüft? (nur bei PET-MRT)
boolean
C3641326 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
Item
MRT-Ausschlusskriterien
integer
C3641326 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
C0680251 (UMLS CUI [1,2])
C0332128 (UMLS CUI [1,3])
C0521116 (UMLS CUI [1,4])
CL Item
DZNE-MRT-Kontraindikationsbogen (1)
CL Item
Kliniküblicher MRT-Patienteneinwilligungsbogen (2)
Item
Medikamenteneinnahme am Untersuchungstag
integer
C0013227 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
C2584899 (UMLS CUI [1,2])
CL Item
Keine (0)
CL Item
Ja (1)
Pharmaceutical preparation
Item
Arzneimittel
text
C0013227 (UMLS CUI [1])
Injected dose
Item
Injizierte Dosis (berechnet)
float
C2986768 (UMLS CUI [1])
Exceeding of permitted maximum dose for FBB scans
Item
Hat die injizierte Aktivität die BfS-genehmigte Maximaldosis für FBB-Scans überschritten?
boolean
C2986768 (UMLS CUI [1,1])
C4296997 (UMLS CUI [1,2])
C0752079 (UMLS CUI [1,3])
C0032743 (UMLS CUI [1,4])
C3818757 (UMLS CUI [1,5])
C4296997 (UMLS CUI [1,2])
C0752079 (UMLS CUI [1,3])
C0032743 (UMLS CUI [1,4])
C3818757 (UMLS CUI [1,5])
Total Dose-Length-Product (only PET-CT)
Item
Gesamt Dosis-Längen-Produkt (DLP) (nur bei PET-CT)
float
C0439810 (UMLS CUI [1,1])
C3539930 (UMLS CUI [1,2])
C1699633 (UMLS CUI [1,3])
C3539930 (UMLS CUI [1,2])
C1699633 (UMLS CUI [1,3])
Medical abnormalities or other special incidents during or after the investigation
Item
Medizinische Auffälligkeiten oder andere besondere Vorkommnisse während oder nach der Untersuchung?
boolean
C0205476 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
Medical abnormalities or other special incidents during or after the investigation - specification
Item
Welche?
text
C0205476 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
C1704258 (UMLS CUI [1,2])
C1707834 (UMLS CUI [1,3])
C4321457 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0205555 (UMLS CUI [2,1])
C1551358 (UMLS CUI [2,2])
C1707834 (UMLS CUI [2,3])
C4321457 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
Evidence of clinical abnormalities in transmission or emission
Item
Hinweise auf nicht studienbezogene klinische Auffälligkeiten in Transmission oder Emission?
boolean
C0332120 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
Evidence of not study-related clinical abnormalities in transmission or emission - specification
Item
Welche?
text
C0332120 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
C0205210 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,3])
C2986746 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0332120 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C1704258 (UMLS CUI [2,3])
C2986834 (UMLS CUI [2,4])
C2348235 (UMLS CUI [2,5])
Notes
Item
Anmerkungen
text
C0947611 (UMLS CUI [1])