Alpha plus thalassemia non deletion type 85422000

SNOMED CT code

SNOMED code

85422000

name

Alpha plus thalassemia non deletion type

status

active

date introduced

2002-01-31

fully specified name(s)

Alpha plus thalassemia non deletion type (disorder)

synonyms

Alpha plus thalassaemia non deletion type
Alpha plus thalassemia non deletion type

attributes - group2

Interprets

Measurement of total hemoglobin concentration 441689006

Has interpretation

Below reference range 281300000

attributes - group1

Interprets

Red blood cell count 14089001

Has interpretation

Below reference range 281300000

attributes - group3

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

parents

Alpha plus thalassemia 36467003
Congenital anemia 63565007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Hereditary hemoglobinopathy 427306008
Thalassemia 40108008
Alpha thalassemia 68913001
Alpha plus thalassemia 36467003
Alpha plus thalassemia non deletion type 85422000

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital anemia 63565007
Alpha plus thalassemia non deletion type 85422000

ancestors

sorted most to least specific

Alpha plus thalassemia 36467003
Congenital anemia 63565007
Alpha thalassemia 68913001
Red blood cell count below reference range 165423001
Thalassemia 40108008
Red blood cell count outside reference range 165427000
Cytopenia 50820005
Anemia due to disturbance of hemoglobin synthesis 14514008
Hereditary hemoglobinopathy 427306008
Red blood cell count - finding 365625004
Blood cell count outside reference range 762656009
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

Disease 64572001

Congenital disease 66091009

Hereditary hemoglobinopathy 427306008

Thalassemia 40108008

Alpha thalassemia 68913001

Alpha plus thalassemia 36467003

Alpha plus thalassemia non deletion type 85422000

SNOMED CT code