Unstable hemoglobin disease 18273004

SNOMED CT code

SNOMED code

18273004

name

Unstable hemoglobin disease

status

active

date introduced

2002-01-31

fully specified name(s)

Unstable hemoglobin disease (disorder)

synonyms

Unstable hemoglobin disease
Congenital Heinz body anemia
Congenital Heinz body anaemia
Unstable haemoglobin disease
CHBHA - Congenital Heinz body hemolytic anemia
Congenital Heinz body hemolytic anemia
CHBHA - Congenital Heinz body haemolytic anaemia
Congenital Heinz body haemolytic anaemia

attributes - group1

Occurrence

Congenital 255399007

Finding site

Erythrocyte 41898006

attributes - group3

Has interpretation

Below reference range 281300000

Interprets

Measurement of total hemoglobin concentration 441689006

attributes - group2

Has interpretation

Below reference range 281300000

Interprets

Red blood cell count 14089001

parents

Hereditary hemoglobinopathy due to globin chain mutation 127038008
Congenital anemia 63565007

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
Unstable hemoglobin disease 18273004

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital anemia 63565007
Unstable hemoglobin disease 18273004

ancestors

sorted most to least specific

Hereditary hemoglobinopathy due to globin chain mutation 127038008
Congenital anemia 63565007
Hereditary hemoglobinopathy 427306008
Hemoglobin below reference range 165397008
Red blood cell count below reference range 165423001
Anemia 271737000
Hereditary red blood cell disorder 414394009
Hemoglobin level outside reference range 441793007
Congenital disease 66091009
Hemoglobinopathy 80141007
Red blood cell count outside reference range 165427000
Cytopenia 50820005
Red blood cell disorder 38292009
Hemoglobin finding 250220000
Hereditary disorder of cellular element of blood 414393003
Red blood cell count - finding 365625004
Measurement finding below reference range 442686002
Hematology test outside reference range 34641000087106
Blood cell count outside reference range 762656009
Hematopoietic system finding 106200001
Hereditary disorder by system 363137000
Disorder of cellular component of blood 414022008
Measurement finding outside reference range 442096005
Protein level - finding 365799007
Disorder of body system 362965005
Hereditary disease 32895009
Finding of blood, lymphatics and immune system 299691001
Finding of substance level 785671009
Genetic disease 782964007
Measurement finding 118245000
Disease 64572001
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

Hereditary hemoglobinopathy due to globin chain mutation 127038008

Unstable hemoglobin disease 18273004

SNOMED CT code