Congenital transferrin deficiency 234353009
SNOMED CT code
| SNOMED code | 234353009 |
|---|---|
| name | Congenital transferrin deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital transferrin deficiency (disorder) |
| synonyms | Congenital transferrin deficiency |
| 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 | |
| children | Congenital atransferrinemia 111571009 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Anemia 271737000 Anemia due to disturbance of hemoglobin synthesis 14514008 Congenital transferrin deficiency 234353009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 Anemia 271737000 Microcytic anemia 234349007 Congenital transferrin deficiency 234353009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital anemia 63565007 Congenital transferrin deficiency 234353009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital transferrin deficiency 234353009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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