Sickle cell-beta-thalassemia 127041004
SNOMED CT code
| SNOMED code | 127041004 |
|---|---|
| name | Sickle cell-beta-thalassemia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Sickle cell-beta-thalassemia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Hematopoietic system structure 57171008 |
| Associated morphology | Drepanocyte 49938009 |
| attributes - group2 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Erythrocyte 41898006 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Hereditary hemoglobinopathy due to globin chain mutation 127038008 Hereditary hemoglobin S 416417002 Sickling disorder due to hemoglobin S 417357006 Double heterozygous sickling disorder 23269001 Sickle cell-beta-thalassemia 127041004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of hematopoietic structure 414027002 Sickle cell-thalassemia disease 36472007 Sickle cell-beta-thalassemia 127041004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Thalassemia 40108008 Beta thalassemia 65959000 Sickle cell-beta-thalassemia 127041004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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