Hereditary spherocytosis due to spectrin deficiency 25266006

SNOMED CT code

SNOMED code

25266006

name

Hereditary spherocytosis due to spectrin deficiency

status

active

date introduced

2002-01-31

fully specified name(s)

Hereditary spherocytosis due to spectrin deficiency (disorder)

synonyms

Hereditary spherocytosis due to spectrin deficiency

attributes - group4

Has interpretation

Present 52101004

Interprets

Hemolysis 404227002

attributes - group1

Associated morphology

Spherocyte 259682008

Finding site

Hematopoietic system structure 57171008

attributes - group2

Has interpretation

Below reference range 281300000

Interprets

Red blood cell count 14089001

attributes - group3

Has interpretation

Below reference range 281300000

Interprets

Measurement of total hemoglobin concentration 441689006

attributes - group5

Finding site

Erythrocyte 41898006

parents

Disorder of hematopoietic structure 414027002
Hereditary spherocytosis 55995005

children

Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin 47516005
Mild hereditary spherocytosis due to spectrin deficiency 32648007
Severe hereditary spherocytosis due to spectrin deficiency 77413008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of hematopoietic structure 414027002
Hereditary spherocytosis due to spectrin deficiency 25266006

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Hereditary spherocytosis 55995005
Hereditary spherocytosis due to spectrin deficiency 25266006

ancestors

sorted most to least specific

Disorder of hematopoietic structure 414027002
Hereditary spherocytosis 55995005
Anemia due to membrane defect 111575000
Autosomal hereditary disorder 1899006
Erythrocyte membrane abnormality 234409003
Hereditary hemolytic anemia 38911009
Anemia due to intrinsic red cell abnormality 323666000
Hemoglobin below reference range 165397008
Hemolytic anemia 61261009
Hereditary red blood cell disorder 414394009
Anemia 271737000
Red blood cell disorder 38292009
Hemoglobin level outside reference range 441793007
Hemolytic disorder 128086004
Red blood cell count below reference range 165423001
Hereditary disorder of cellular element of blood 414393003
Disorder of cellular component of blood 414022008
Hemoglobin finding 250220000
Hematology test outside reference range 34641000087106
Red blood cell count outside reference range 165427000
Hemolysis 73320003
Hereditary disorder by system 363137000
Cytopenia 50820005
Disorder of body system 362965005
Hereditary disease 32895009
Hematopoietic system finding 106200001
Measurement finding below reference range 442686002
Protein level - finding 365799007
Red blood cell count - finding 365625004
Red blood cell destruction finding 127403002
Blood cell count outside reference range 762656009
Finding of blood, lymphatics and immune system 299691001
Genetic disease 782964007
Measurement finding outside reference range 442096005
Finding of substance level 785671009
Functional finding 118228005
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

Disorder of body system 362965005

Disorder of hematopoietic structure 414027002

Hereditary spherocytosis due to spectrin deficiency 25266006

SNOMED CT code