HPFH deletion type 85557000
SNOMED CT code
SNOMED code | 85557000 |
---|---|
name | HPFH deletion type |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary persistence of fetal hemoglobin deletion type (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 | Hereditary persistence of fetal hemoglobin thalassemia 16964007 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Thalassemia 40108008 Hereditary persistence of fetal hemoglobin thalassemia 16964007 HPFH deletion type 85557000 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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