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SNOMED CT
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/SNOMEDCT/128113003
http://purl.bioontology.org/ontology/SNOMEDCT/128113003
|
|---|---|
| Preferred Name | Hereditary von Willebrand disease type 1B |
| Synonyms |
Hereditary von Willebrand disease type 1B (disorder)
von Willebrand disease type IB
Hereditary von Willebrand disease type IB
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Hereditary von Willebrand disease type 1B (disorder)
von Willebrand disease type IB
Hereditary von Willebrand disease type IB
|
|---|---|
| prefLabel | Hereditary von Willebrand disease type 1B
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID |
900000000000020002
900000000000017005
|
| notation | 128113003
|
| Effective time | 20020131
|
| Active | 1
|
| INACTIVATION INDICATOR | 900000000000483008
|
| interprets | |
| subClassOf | |
| Semantic type UMLS property | |
| Has interpretation | |
| type | |
| Subset member |
447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~D68.0
6011000124106~MAPGROUP~1
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
6011000124106~MAPTARGET~D68.01
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPADVICE~ALWAYS D68.0
6011000124106~MAPADVICE~ALWAYS D68.0
900000000000497000~MAPTARGET~XU76E
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~D68.0
6011000124106~MAPADVICE~ALWAYS D68.01
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
900000000000490003~VALUEID~900000000000483008
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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|
| DEFINITION STATUS ID | 900000000000074008
|
| tui | T047
|
| CTV3ID | XU76E
|
| cui | C1264042
|
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