Congenital atransferrinemia 111571009
SNOMED CT code
SNOMED code | 111571009 |
---|---|
name | Congenital atransferrinemia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital atransferrinemia (disorder) |
synonyms |
|
attributes - group3 | |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Has interpretation | Below reference range 281300000 |
Interprets | Red blood cell count 14089001 |
attributes - group2 | |
Has interpretation | Below reference range 281300000 |
Interprets | Measurement of total hemoglobin concentration 441689006 |
attributes - group4 | |
Interprets | Red blood cell size determination 165472008 |
parents | Congenital transferrin deficiency 234353009 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital anemia 63565007 Congenital transferrin deficiency 234353009 Congenital atransferrinemia 111571009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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