HPFH A gamma beta^+^ thalassemia 39586009
SNOMED CT code
SNOMED code | 39586009 |
---|---|
name | HPFH A gamma beta^+^ thalassemia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) |
synonyms |
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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 | |
children | A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis 5967006 |
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 A gamma beta^+^ thalassemia 39586009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Thalassemia 40108008 Beta thalassemia 65959000 Beta plus thalassemia 79592006 HPFH A gamma beta^+^ thalassemia 39586009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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