Thalassemia 40108008

SNOMED CT code

SNOMED code

40108008

name

Thalassemia

status

active

date introduced

2002-01-31

fully specified name(s)

Thalassemia (disorder)

synonyms

Hereditary leptocytosis
Thalassaemia
Thalassemia

attributes - group2

Interprets

Measurement of total hemoglobin concentration 441689006

Has interpretation

Below reference range 281300000

attributes - group3

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Anemia due to disturbance of hemoglobin synthesis 14514008
Hereditary hemoglobinopathy 427306008

children

[X]Other thalassemias 191418000 removed: 2009-01-31
Acquired hemoglobin H disease 307343001
Alpha thalassemia 68913001
Alpha thalassemia-mental retardation syndrome 277918006 removed: 2018-01-31
Alpha-beta thalassemia 234389001
Beta thalassemia 65959000
Delta thalassemia 16427007
Gamma thalassemia 234390005
Hb Lepore thalassemia 69216008
Hereditary persistence of fetal hemoglobin thalassemia 16964007
Heterozygous thalassemia 19442009
Thalassemia in mother complicating childbirth 10806241000119108
Thalassemia in mother complicating pregnancy 72331000119105
Thalassemia intermedia 934007
Thalassemia major 75451007
Thalassemia major NEC 267520000 removed: 2010-01-31
Thalassemia minor 68875002 removed: 2008-07-31
Thalassemia NOS 267521001 removed: 2010-01-31
Thalassemia syndrome 84188003
Thalassemia with other hemoglobinopathy 47047009

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 disturbance of hemoglobin synthesis 14514008
Thalassemia 40108008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Thalassemia 40108008

ancestors

sorted most to least specific

Anemia due to disturbance of hemoglobin synthesis 14514008
Hereditary hemoglobinopathy 427306008
Hemoglobin below reference range 165397008
Hereditary red blood cell disorder 414394009
Anemia 271737000
Congenital disease 66091009
Hemoglobinopathy 80141007
Hemoglobin level outside reference range 441793007
Red blood cell disorder 38292009
Measurement finding below reference range 442686002
Hereditary disorder of cellular element of blood 414393003
Hemoglobin finding 250220000
Disorder of cellular component of blood 414022008
Measurement finding outside reference range 442096005
Hematology test outside reference range 34641000087106
Hereditary disorder by system 363137000
Hematopoietic system finding 106200001
Disorder of body system 362965005
Finding of blood, lymphatics and immune system 299691001
Protein level - finding 365799007
Hereditary disease 32895009
Finding of substance level 785671009
Genetic disease 782964007
Disease 64572001
Measurement finding 118245000
Evaluation finding 441742003
Procedure related finding 127325009
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 disturbance of hemoglobin synthesis 14514008

Thalassemia 40108008

SNOMED CT code