| Niveau/ Type |
Code |
Weergavenaam |
Codesysteem |
| 0‑L |
128105004
|
von Willebrand disorder (disorder)
|
SNOMED CT |
| 0‑L |
90935002
|
Hemophilia (disorder)
|
SNOMED CT |
| 0‑L |
302215000
|
Thrombocytopenic disorder (disorder)
|
SNOMED CT |
| 0‑L |
67406007
|
Disseminated intravascular coagulation (disorder)
|
SNOMED CT |
| 0‑S |
234467004
|
Thrombophilia (disorder)
|
SNOMED CT |
| 1‑L |
36351005
|
Antithrombin III deficiency (disorder)
|
SNOMED CT |
| 1‑L |
76407009
|
Protein C deficiency disease (disorder)
|
SNOMED CT |
| 1‑L |
1563006
|
Protein S deficiency disease (disorder)
|
SNOMED CT |
| 1‑L |
307116001
|
Heterozygous Factor V Leiden mutation (disorder)
|
SNOMED CT |
| 1‑L |
307115002
|
Homozygous Factor V Leiden mutation (disorder)
|
SNOMED CT |
| 1‑L |
46981006
|
Factor XII deficiency disease (disorder)
|
SNOMED CT |
| 0‑L |
128053003
|
Deep venous thrombosis (disorder)
|
SNOMED CT |
| 0‑L |
59282003
|
Pulmonary embolism (disorder)
|
SNOMED CT |
|
| 0‑L |
OTH
|
Overig
|
NullFlavor |
Waardelijst Type stollingsprobleem 2014‑08‑14 14:42:07
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