Hemoglobin SS disease with vasoocclusive crisis 440206000

SNOMED CT code

SNOMED code

440206000

name

Hemoglobin SS disease with vasoocclusive crisis

status

active

date introduced

2009-01-31

fully specified name(s)

Hemoglobin SS disease with vasoocclusive crisis (disorder)

synonyms

Hemoglobin SS disease with vasoocclusive crisis
Haemoglobin SS disease with vasoocclusive crisis

attributes - group1

Interprets

Measurement of total hemoglobin concentration 441689006

Has interpretation

Below reference range 281300000

attributes - group5

Associated morphology

Drepanocyte 49938009

attributes - group4

Causative agent

Hemoglobin S 50095005

attributes - group3

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Hemoglobin SS disease with crisis 417425009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of blood, lymphatics and immune system 299691001
Disorder of cellular component of blood 414022008
Anemia 271737000
Anemia due to intrinsic red cell abnormality 323666000
Hb S disease 127040003
Hemoglobin SS disease with crisis 417425009
Hemoglobin SS disease with vasoocclusive crisis 440206000

ancestors

sorted most to least specific

Hemoglobin SS disease with crisis 417425009
Hb S disease 127040003
Hemoglobin S sickling disorder with crisis 417279003
Homozygous hemoglobinopathy 123772008
Sickling disorder due to hemoglobin S 417357006
Anemia due to disturbance of hemoglobin synthesis 14514008
Anemia due to intrinsic red cell abnormality 323666000
Hereditary hemoglobin S 416417002
Hemoglobin below reference range 165397008
Anemia 271737000
Hereditary hemoglobinopathy due to globin chain mutation 127038008
Hemoglobin level outside reference range 441793007
Measurement finding below reference range 442686002
Hereditary hemoglobinopathy 427306008
Hemoglobin finding 250220000
Measurement finding outside reference range 442096005
Hematology test outside reference range 34641000087106
Hereditary red blood cell disorder 414394009
Hematopoietic system finding 106200001
Congenital disease 66091009
Hemoglobinopathy 80141007
Protein level - finding 365799007
Red blood cell disorder 38292009
Hereditary disorder of cellular element of blood 414393003
Finding of substance level 785671009
Disorder of cellular component of blood 414022008
Hereditary disorder by system 363137000
Measurement finding 118245000
Disorder of body system 362965005
Evaluation finding 441742003
Finding of blood, lymphatics and immune system 299691001
Hereditary disease 32895009
Procedure related finding 127325009
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Finding of blood, lymphatics and immune system 299691001

Disorder of cellular component of blood 414022008

Anemia 271737000

Anemia due to intrinsic red cell abnormality 323666000

Hb S disease 127040003

Hemoglobin SS disease with crisis 417425009

Hemoglobin SS disease with vasoocclusive crisis 440206000

SNOMED CT code