Hereditary hemoglobin S 416417002
SNOMED CT code
SNOMED code | 416417002 |
---|---|
name | Hereditary hemoglobin S |
status | active |
date introduced | 2005-07-31 |
fully specified name(s) | Hereditary hemoglobin S (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Erythrocyte 41898006 |
parents | Hereditary hemoglobinopathy due to globin chain mutation 127038008 |
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 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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