loading...| Preferred Name |
Hereditary factor XI deficiency disease |
|
| Synonyms |
Congenital factor XI deficiency disease Hereditary factor XI deficiency disease (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/49762007 |
|
| Active |
1 |
|
| 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) |
|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 900000000000017005 |
|
| CTV3ID |
D302. |
|
| cui |
C0015523 |
|
| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20180731 |
|
| Has interpretation | ||
| INACTIVATION INDICATOR |
723278000 |
|
| interprets | ||
| notation |
49762007 |
|
| Occurs in | ||
| prefLabel |
Hereditary factor XI deficiency disease |
|
| 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 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/66091009 http://purl.bioontology.org/ontology/SNOMEDCT/85995004 http://purl.bioontology.org/ontology/SNOMEDCT/90935002 |