SNOMED CT

Last uploaded: January 16, 2025
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Id http://purl.bioontology.org/ontology/SNOMEDCT/40855001
http://purl.bioontology.org/ontology/SNOMEDCT/40855001
Preferred Name

Hereditary factor VII deficiency disease
Synonyms
Hereditary hypoproconvertinemia
Hereditary factor VII deficiency disease (disorder)
Hereditary factor VII deficiency syndrome
Hereditary hypoproconvertinaemia
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
Hereditary hypoproconvertinemia
Hereditary factor VII deficiency disease (disorder)
Hereditary factor VII deficiency syndrome
Hereditary hypoproconvertinaemia
prefLabel
Hereditary factor VII deficiency disease
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000020002
900000000000448009
notation
40855001
Effective time
20020131
Active
1
interprets
subClassOf
Semantic type UMLS property
Has interpretation
type
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~D68.2
6011000124106~MAPGROUP~1
447562003~MAPADVICE~ALWAYS D68.2
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~D68.2
900000000000497000~MAPTARGET~XUDVW
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPADVICE~ALWAYS D68.2
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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DEFINITION STATUS ID
900000000000074008
tui
T047
CTV3ID
XUDVW
cui
C0272320
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