SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/38323006
http://purl.bioontology.org/ontology/SNOMEDCT/38323006
Preferred Name

Fetal warfarin syndrome
Synonyms
Dysmorphism due to warfarin
Foetal warfarin syndrome
Fetal warfarin syndrome (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

prefLabel
Fetal warfarin syndrome
altLabel
Dysmorphism due to warfarin
Foetal warfarin syndrome
Fetal warfarin syndrome (disorder)
Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Effective time
20200131
cui
C0265374
Has pathological process
CTV3ID
X78ED
DEFINITION STATUS ID
900000000000073002
CASE SIGNIFICANCE ID
900000000000448009
Occurs in
tui
T047
Active
1
Has associated morphology
notation
38323006
type
subClassOf
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPGROUP~1
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPTARGET~P04.1
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~ALWAYS Q86.2
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~Q86.2
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
900000000000497000~MAPTARGET~X78ED
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
447562003~MAPADVICE~ALWAYS P04.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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Has causative agent
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