Hemoglobin S sickling disorder with crisis 417279003

SNOMED CT code

SNOMED code

417279003

name

Hemoglobin S sickling disorder with crisis

status

active

date introduced

2005-07-31

fully specified name(s)

Hemoglobin S sickling disorder with crisis (disorder)

synonyms

Hemoglobin S sickling disorder with crisis
Haemoglobin S sickling disorder with crisis
Sickle cell anemia crisis
Sickle cell anaemia crisis

attributes - group1

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Sickling disorder due to hemoglobin S 417357006

children

Hemoglobin SS disease with crisis 417425009
Sickle cell-hemoglobin C disease with crisis 417517009
Sickle cell-hemoglobin D disease with crisis 417748003
Sickle cell-hemoglobin E disease with crisis 416484003
Sickle cell-thalassemia disease with crisis 416826005

hierarchies

a selection of possible paths

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
Hemoglobin S sickling disorder with crisis 417279003

ancestors

sorted most to least specific

Sickling disorder due to hemoglobin S 417357006
Hereditary hemoglobin S 416417002
Hereditary hemoglobinopathy due to globin chain mutation 127038008
Hereditary hemoglobinopathy 427306008
Hereditary red blood cell disorder 414394009
Congenital disease 66091009
Hemoglobinopathy 80141007
Red blood cell disorder 38292009
Hereditary disorder of cellular element of blood 414393003
Hereditary disorder by system 363137000
Disorder of cellular component of blood 414022008
Disorder of body system 362965005
Hereditary disease 32895009
Finding of blood, lymphatics and immune system 299691001
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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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

Hemoglobin S sickling disorder with crisis 417279003

SNOMED CT code