Wiskott-Aldrich autosomal dominant variant syndrome 403837005

SNOMED CT code

SNOMED code

403837005

name

Wiskott-Aldrich autosomal dominant variant syndrome

status

active

date introduced

2003-07-31

fully specified name(s)

Wiskott-Aldrich autosomal dominant variant syndrome (disorder)

synonyms

Wiskott-Aldrich autosomal dominant variant syndrome

attributes - group2

Has interpretation

Abnormal 263654008

Interprets

Hemostatic function 74848003

attributes - group4

Occurrence

Congenital 255399007

attributes - group5

Pathological process

Abnormal immune process 769247005

attributes - group3

Finding site

Immune system structure 116003000

attributes - group1

Has interpretation

Below reference range 281300000

Interprets

Platelet count 61928009

parents

Wiskott-Aldrich syndrome 36070007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of immune function 414029004
Immune thrombocytopenia 2897005
Wiskott-Aldrich syndrome 36070007
Wiskott-Aldrich autosomal dominant variant syndrome 403837005

ancestors

sorted most to least specific

Wiskott-Aldrich syndrome 36070007
Dense body defect 234474009
Immunodeficiency associated with multiple organ system abnormalities 234641000
Immune thrombocytopenia 2897005
Congenital immunodeficiency disease 36138009
Hereditary disorder of immune system 363138005
Hereditary thrombocytopenic disorder 438492008
Hereditary cancer-predisposing syndrome 699346009
Congenital thrombocytopenia 737221003
Platelet storage pool defect 128099001
Immunodeficiency with major anomalies 234631003
Thrombocytopenic disorder 302215000
Hereditary platelet function disorder 128096008
Disorder of immune structure 414030009
Congenital disease 66091009
Primary immune deficiency disorder 58606001
Platelet count below reference range 415116008
Inherited platelet disorder 234469001
Immunodeficiency disorder 234532001
Qualitative platelet disorder 267532001
Platelet count outside reference range 165558001
Cytopenia 50820005
Platelet disorder 22716005
Disorder of immune function 414029004
Hereditary disorder of cellular element of blood 414393003
Platelet count - finding 365632008
Measurement finding below reference range 442686002
Blood cell count outside reference range 762656009
Disorder of hemostatic system 362970003
Hereditary disorder by system 363137000
Disorder of cellular component of blood 414022008
Measurement finding outside reference range 442096005
Hemostatic system finding 128153000
Functional finding 118228005
Disorder of body system 362965005
Hereditary disease 32895009
Finding of blood, lymphatics and immune system 299691001
Measurement finding 118245000
Hematopoietic system finding 106200001
Genetic disease 782964007
Evaluation finding 441742003
Disease 64572001
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 immune function 414029004

Immune thrombocytopenia 2897005

Wiskott-Aldrich syndrome 36070007

Wiskott-Aldrich autosomal dominant variant syndrome 403837005

SNOMED CT code