Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome 783254003
SNOMED CT code
| SNOMED code | 783254003 |
|---|---|
| name | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Erythrocyte 41898006 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Hereditary persistence of fetal hemoglobin 191201002 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome 783254003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary hemoglobinopathy 427306008 Hereditary hemoglobinopathy due to globin chain mutation 127038008 Hereditary hemoglobin S 416417002 Sickling disorder due to hemoglobin S 417357006 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome 783254003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome 783254003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com