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SNOMED CT
Last uploaded:
January 16, 2025
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| Preferred Name | Hereditary factor V deficiency disease | |
| Synonyms |
Parahaemophilia Hereditary hypoproaccelerinemia Owren's disease AC globulin deficiency Hereditary hypoproaccelerinaemia Hereditary factor V deficiency disease (disorder) Parahemophilia |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/88776002 |
|
| Active |
1
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|
| altLabel |
Parahaemophilia Hereditary hypoproaccelerinemia Owren's disease AC globulin deficiency Hereditary hypoproaccelerinaemia Hereditary factor V deficiency disease (disorder) Parahemophilia
|
|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005
|
|
| CTV3ID |
XUN2V
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|
| cui |
C0015499
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|
| DEFINITION STATUS ID |
900000000000074008
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|
| Effective time |
20020131
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|
| Has interpretation | ||
| INACTIVATION INDICATOR |
900000000000494007
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| interprets | ||
| notation |
88776002
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|
| prefLabel |
Hereditary factor V deficiency disease
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|
| Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPTARGET~D68.2 900000000000490003~VALUEID~900000000000494007 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 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 900000000000531004~TARGETCOMPONENT~4320005 6011000124106~MAPADVICE~ALWAYS D68.2 900000000000497000~MAPTARGET~XUN2V 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~TRUE 900000000000531004~TARGETCOMPONENT~366160003 900000000000509007~ACCEPTABILITYID~900000000000549004
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|
| tui |
T047
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|
| Type ID |
900000000000003001 900000000000013009
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| subClassOf |
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