Preferred Name |
Prothrombin complex deficiency |
|
Synonyms |
Prothrombin complex deficiency (disorder) |
|
ID |
http://purl.bioontology.org/ontology/SNOMEDCT/234454002 |
|
Active |
1 |
|
altLabel |
Prothrombin complex deficiency (disorder) |
|
CASE SIGNIFICANCE ID |
900000000000448009 |
|
CTV3ID |
X20EU |
|
cui |
C0398615 |
|
DEFINITION STATUS ID |
900000000000074008 |
|
Effective time |
20020131 |
|
Has interpretation | ||
interprets | ||
notation |
234454002 |
|
prefLabel |
Prothrombin complex deficiency |
|
Subset member |
6011000124106~MAPADVICE~IF ACQUIRED FACTOR II DEFICIENCY CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 2036003 | Acquired factor VII deficiency disease | 6011000124106~MAPRULE~IFA 191298004 | Acquired factor II deficiency (disorder) | 447562003~MAPRULE~TRUE 6011000124106~MAPADVICE~IF FACTOR X DEFICIENCY DUE TO SYSTEMIC AMYLOIDOSIS CHOOSE E85.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~4 6011000124106~MAPTARGET~D68.2 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPADVICE~IF ACQUIRED FACTOR X DEFICIENCY DISEASE CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPRULE~IFA 33820001 | Acquired factor X deficiency disease | 6011000124106~MAPGROUP~2 6011000124106~MAPTARGET~E85.9 447562003~MAPADVICE~ALWAYS D68.2 | MAPPED FOLLOWING WHO GUIDANCE 6011000124106~MAPRULE~IFA 33820001 | Acquired factor X deficiency disease (disorder) | 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPADVICE~IF FACTOR X DEFICIENCY DUE TO SYSTEMIC AMYLOIDOSIS CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 447562003~MAPTARGET~D68.2 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPADVICE~ALWAYS D68.2 6011000124106~MAPADVICE~IF ACQUIRED FACTOR VII DEFICIENCY DISEASE CHOOSE D68.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 191298004 | Acquired factor II deficiency | 6011000124106~MAPRULE~IFA 2036003 | Acquired factor VII deficiency disease (disorder) | 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~TRUE 900000000000497000~MAPTARGET~X20EU 6011000124106~MAPPRIORITY~3 6011000124106~MAPPRIORITY~2 6011000124106~MAPTARGET~D68.4 6011000124106~MAPRULE~IFA 1148862002 | Factor X deficiency due to systemic amyloidosis | |
|
tui |
T047 |
|
Type ID |
900000000000003001 900000000000013009 |
|
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/RCD/X20EU | RCD | CUI | |
http://purl.bioontology.org/ontology/SCTSPA/234454002 | SCTSPA | CUI | |
http://sbmi.uth.tmc.edu/ontology/ochv#C0398615 | OCHV | LOOM | |
http://purl.bioontology.org/ontology/RCD/X20EU | RCD | LOOM |