loading...| Preferred Name |
Genetic anomaly of leukocyte |
|
| Synonyms |
Genetic anomaly of leukocyte (disorder) Genetic leucocyte disorder |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/47986005 |
|
| Active |
1 |
|
| altLabel |
Genetic anomaly of leukocyte (disorder) Genetic anomaly of leucocyte Genetic leukocyte disorder Genetic leucocyte disorder |
|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 |
|
| CTV3ID |
XUEum |
|
| cui |
C0017377 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has pathological process | ||
| interprets | ||
| notation |
47986005 |
|
| prefLabel |
Genetic anomaly of leukocyte |
|
| Subset member |
447562003~MAPRULE~TRUE 900000000000497000~MAPTARGET~XUEum 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPADVICE~IF SHORT STATURE, OPTIC NERVE ATROPHY, PELGER-HUËT ANOMALY SYNDROME CHOOSE H47.22 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~D72.0 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 447562003~MAPADVICE~ALWAYS D72.0 6011000124106~MAPRULE~IFA 1237618009 | Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome | 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPADVICE~IF SHORT STATURE, OPTIC NERVE ATROPHY, PELGER-HUËT ANOMALY SYNDROME CHOOSE R62.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~R62.52 6011000124106~MAPPRIORITY~1 447562003~MAPTARGET~D72.0 6011000124106~CORRELATIONID~447561005 6011000124106~MAPADVICE~ALWAYS D72.0 6011000124106~MAPTARGET~H47.22 6011000124106~MAPRULE~TRUE 6011000124106~MAPGROUP~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 6011000124106~MAPADVICE~IF SHORT STATURE, OPTIC NERVE ATROPHY, PELGER-HUËT ANOMALY SYNDROME CHOOSE D72.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |