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SNOMED CT
Last uploaded:
August 28, 2024
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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) |
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ID |
http://purl.bioontology.org/ontology/SNOMEDCT/49762007 |
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Active |
1
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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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CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005
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CTV3ID |
D302.
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cui |
C0015523
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DEFINITION STATUS ID |
900000000000073002
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Effective time |
20180731
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Has interpretation | ||
INACTIVATION INDICATOR |
723278000
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interprets | ||
notation |
49762007
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Occurs in | ||
prefLabel |
Hereditary factor XI deficiency disease
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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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tui |
T047
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Type ID |
900000000000003001 900000000000013009
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subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/66091009 http://purl.bioontology.org/ontology/SNOMEDCT/85995004 http://purl.bioontology.org/ontology/SNOMEDCT/90935002 |
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