Hemoglobin H disease 48553001
SNOMED CT code
SNOMED code | 48553001 |
---|---|
name | Hemoglobin H disease |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hemoglobin H disease (disorder) |
synonyms |
|
attributes - group2 | |
Interprets | Measurement of total hemoglobin concentration 441689006 |
Has interpretation | Below reference range 281300000 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Erythrocyte 41898006 |
parents | Alpha thalassemia 68913001 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Thalassemia 40108008 Alpha thalassemia 68913001 Hemoglobin H disease 48553001 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.