Hemoglobin E/beta thalassemia disease 234392002
SNOMED CT code
| SNOMED code | 234392002 |
|---|---|
| name | Hemoglobin E/beta thalassemia disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hemoglobin E/beta thalassemia disease (disorder) |
| synonyms |
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| attributes - group2 | |
| Interprets | Measurement of total hemoglobin concentration 441689006 |
| Has interpretation | Below reference range 281300000 |
| attributes - group1 | |
| 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 Hemoglobin E disease 25065001 Hemoglobin E/beta thalassemia disease 234392002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Thalassemia 40108008 Beta thalassemia 65959000 Hemoglobin E/beta thalassemia disease 234392002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hemoglobin E/beta thalassemia disease 234392002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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