Sickle cell trait 16402000

SNOMED CT code

SNOMED code

16402000

name

Sickle cell trait

status

active

date introduced

2002-01-31

fully specified name(s)

Sickle cell trait (disorder)

synonyms

AS - Sickle cell trait
Heterozygous for Hb S
Drepanocytosis
RBC's - sickle cells present
Sickle cells present
Sickle cell trait
Hemoglobin S-A disorder
Hemoglobin A-S genotype
Hemoglobin S trait
Heterozygous hemoglobin S
Haemoglobin A-S genotype
Haemoglobin S-A disorder
Haemoglobin S trait
Heterozygous haemoglobin S

attributes - group1

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Heterozygous hemoglobinopathy 123773003
Hereditary hemoglobin S 416417002

children

Sickle cell trait in mother complicating childbirth 10759401000119105
Sickle cell trait in mother complicating pregnancy 72321000119107
Sickle cell trait with coexistent alpha-thalassemia 127046009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Heterozygous hemoglobinopathy 123773003
Sickle cell trait 16402000

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
Sickle cell trait 16402000

ancestors

sorted most to least specific

Heterozygous hemoglobinopathy 123773003
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

Heterozygous hemoglobinopathy 123773003

Sickle cell trait 16402000

SNOMED CT code