Niveau/ Type |
Code |
Weergavenaam |
Codesysteem |
0‑L |
275978004
|
Screening for malignant neoplasm of colon (procedure)
|
SNOMED Clinical Terms |
0‑L |
43364001
|
Abdominal discomfort (finding)
|
SNOMED Clinical Terms |
0‑L |
12063002
|
Rectal hemorrhage (disorder)
|
SNOMED Clinical Terms |
0‑L |
35240004
|
Iron deficiency (disorder)
|
SNOMED Clinical Terms |
0‑L |
167669009
|
Fecal occult blood: positive (finding)
|
SNOMED Clinical Terms |
0‑L |
236071009
|
Chronic diarrhea (disorder)
|
SNOMED Clinical Terms |
0‑L |
88111009
|
Altered bowel function (finding)
|
SNOMED Clinical Terms |
0‑L |
225419007:408730004=429047008
|
Surveillance - Procedure context (attribute) = History of adenomatous polyp of colon
(situation)
|
SNOMED Clinical Terms |
0‑L |
225419007:408730004=429699009
|
Surveillance - Procedure context (attribute) = History of malignant neoplasm of colon
(situation)
|
SNOMED Clinical Terms |
0‑L |
225419007:408730004=608844008
|
Surveillance - Procedure context (attribute) = History of inflammatory bowel disease
(situation)
|
SNOMED Clinical Terms |
0‑L |
24526004
|
Inflammatory bowel disease (disorder)
|
SNOMED Clinical Terms |
0‑L |
429969003
|
Family history of polyp of colon (situation)
|
SNOMED Clinical Terms |
0‑L |
1421000119104
|
Family history of colorectal cancer (situation)
|
SNOMED Clinical Terms |
0‑L |
160381001:246090004=315058005
|
Family history: Gastrointestinal disease (situation) - Associated finding (attribute)
= Hereditary nonpolyposis colon cancer (disorder)
|
SNOMED Clinical Terms |
0‑L |
160381001
|
Family history: Gastrointestinal disease (situation)
|
SNOMED Clinical Terms |
0‑L |
119523007
|
Disorder of large intestine (disorder)
|
SNOMED Clinical Terms |
|