Sickling disorder due to hemoglobin S 417357006

SNOMED CT code

SNOMED code

417357006

name

Sickling disorder due to hemoglobin S

status

active

date introduced

2005-07-31

fully specified name(s)

Sickling disorder due to hemoglobin S (disorder)

synonyms

Sickling disorder due to hemoglobin S
Sickling disorder due to haemoglobin S
Sickle cell disease
Sickle cell syndrome

attributes - group1

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Hereditary hemoglobin S 416417002

children

Double heterozygous sickling disorder 23269001
Hb S disease 127040003
Hemoglobin S sickling disorder with crisis 417279003
Hemoglobin S sickling disorder without crisis 416290001
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome 783254003
Sickle cell-thalassemia disease 36472007

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

ancestors

sorted most to least specific

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

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

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

SNOMED CT code