loading...| Preferred Name |
Protein C deficiency disease |
|
| Synonyms |
Protein C deficiency disease (disorder) Protein C deficiency |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/76407009 |
|
| Active |
1 |
|
| altLabel |
Protein C deficiency disease (disorder) Protein C deficiency |
|
| Associated finding of |
http://purl.bioontology.org/ontology/SNOMEDCT/109001000119105 |
|
| CASE SIGNIFICANCE ID |
900000000000020002 |
|
| CTV3ID |
X20El |
|
| cui |
C0398625 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has interpretation | ||
| interprets | ||
| notation |
76407009 |
|
| prefLabel |
Protein C deficiency disease |
|
| Subset member |
6011000124106~MAPRULE~IFA 439002002 | Thrombophilia due to acquired protein C deficiency (disorder) | 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 402851000 | Neonatal purpura fulminans (homozygous protein C deficiency) | 6011000124106~MAPGROUP~1 447562003~MAPADVICE~IF NEONATAL PURPURA FULMINANS (HOMOZYGOUS PROTEIN C DEFICIENCY) CHOOSE P60 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF THROMBOPHILIA DUE TO ACQUIRED PROTEIN C DEFICIENCY CHOOSE D68.69 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPTARGET~D68.5 6011000124106~MAPADVICE~IF NEONATAL PURPURA FULMINANS DUE TO HOMOZYGOUS PROTEIN C DEFICIENCY CHOOSE P60 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 6011000124106~MAPTARGET~D68.59 447562003~CORRELATIONID~447561005 447562003~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447637006 6011000124106~MAPTARGET~P60 900000000000509007~ACCEPTABILITYID~900000000000548007 447562003~MAPADVICE~ALWAYS D68.5 447562003~MAPTARGET~P60 6011000124106~MAPADVICE~IF NEONATAL PURPURA FULMINANS (HOMOZYGOUS PROTEIN C DEFICIENCY) CHOOSE P60 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF NEONATAL PURPURA FULMINANS CHOOSE P60 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 439002002 | Thrombophilia due to acquired protein C deficiency | 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 402851000 | Neonatal purpura fulminans (homozygous protein C deficiency) (disorder) | 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447639009 900000000000497000~MAPTARGET~X20El 6011000124106~MAPRULE~IFA 402851000 | Neonatal purpura fulminans due to homozygous protein C deficiency | 6011000124106~MAPTARGET~D68.69 447562003~MAPCATEGORYID~447639009 6011000124106~MAPADVICE~ALWAYS D68.59 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 447562003~MAPRULE~IFA 402851000 | Neonatal purpura fulminans (homozygous protein C deficiency) (disorder) | 447562003~MAPPRIORITY~2 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |