Hemoglobin E disease 25065001
SNOMED CT code
SNOMED code | 25065001 |
---|---|
name | Hemoglobin E disease |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hemoglobin E disease (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Erythrocyte 41898006 |
parents | Hereditary hemoglobinopathy due to globin chain mutation 127038008 |
children | Hemoglobin E/beta thalassemia disease 234392002 |
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 |
ancestors | sorted most to least specific
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cpt crosswalks |
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