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SNOMED CT

Last uploaded: January 16, 2025
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Id http://purl.bioontology.org/ontology/SNOMEDCT/33905008
http://purl.bioontology.org/ontology/SNOMEDCT/33905008
Preferred Name

Hereditary spherocytosis due to deficiency of protein 4.2
Synonyms
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)
prefLabel
Hereditary spherocytosis due to deficiency of protein 4.2
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000448009
notation
33905008
Effective time
20020131
Active
1
Has finding site
interprets
subClassOf
Semantic type UMLS property
Has interpretation
type
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~D58.0
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~R71.8
6011000124106~MAPADVICE~ALWAYS D58.0
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
900000000000497000~MAPTARGET~XUC41
447562003~MAPADVICE~ALWAYS D58.0
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
447562003~MAPTARGET~D58.0
6011000124106~MAPRULE~TRUE
6011000124106~MAPADVICE~ALWAYS R71.8
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DEFINITION STATUS ID
900000000000074008
tui
T047
CTV3ID
XUC41
cui
C0272038
Has associated morphology
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