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SNOMED CT
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/SNOMEDCT/49762007
http://purl.bioontology.org/ontology/SNOMEDCT/49762007
|
|---|---|
| Preferred Name | Hereditary factor XI deficiency disease |
| Synonyms |
Congenital factor XI deficiency disease
Plasma thromboplastin antecedent deficiency
Hemophilia C
PTA deficiency
Rosenthal's disease
Thromboplastin antecedent deficiency
Haemophilia C
Hereditary factor XI deficiency disease (disorder)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Congenital factor XI deficiency disease
Plasma thromboplastin antecedent deficiency
Hemophilia C
PTA deficiency
Rosenthal's disease
Thromboplastin antecedent deficiency
Haemophilia C
Hereditary factor XI deficiency disease (disorder)
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|
|---|---|
| prefLabel | Hereditary factor XI deficiency disease
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID |
900000000000020002
900000000000448009
900000000000017005
|
| notation | 49762007
|
| Effective time | 20180731
|
| Active | 1
|
| INACTIVATION INDICATOR | 723278000
|
| interprets | |
| subClassOf | |
| Semantic type UMLS property | |
| Has interpretation | |
| type | |
| Subset member |
447562003~MAPRULE~TRUE
900000000000497000~MAPTARGET~D302.
900000000000531004~TARGETCOMPONENT~767713001
6011000124106~MAPTARGET~D68.1
6011000124106~MAPGROUP~1
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~D68.1
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPPRIORITY~1
900000000000490003~VALUEID~723278000
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~ALWAYS D68.1
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
447562003~MAPADVICE~ALWAYS D68.1
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|
| DEFINITION STATUS ID | 900000000000073002
|
| tui | T047
|
| CTV3ID | D302.
|
| Occurs in | |
| cui | C0015523
|
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