Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT code

SNOMED code

190996002

name

Severe combined immunodeficiency with reticular dysgenesis

status

active

date introduced

2002-01-31

fully specified name(s)

Severe combined immunodeficiency with reticular dysgenesis (disorder)

synonyms

Severe combined immunodeficiency with reticular dysgenesis

attributes - group4

Finding site

Immune system structure 116003000

attributes - group5

Occurrence

Congenital 255399007

attributes - group6

Pathological process

Abnormal immune process 769247005

attributes - group1

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

attributes - group3

Has interpretation

Below reference range 281300000

Interprets

Neutrophil count 30630007

parents

SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation 3439009
Disorder of immune structure 414030009
Hereditary white blood cell disorder 414395005
Congenital anemia 63565007
Congenital neutropenia 89655007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital immunodeficiency disease 36138009
Severe combined immunodeficiency disease 31323000
SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation 3439009
Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of immune structure 414030009
Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of blood, lymphatics and immune system 299691001
Disorder of cellular component of blood 414022008
White blood cell disorder 54097007
Hereditary white blood cell disorder 414395005
Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital anemia 63565007
Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital immunodeficiency disease 36138009
Congenital neutropenia 89655007
Severe combined immunodeficiency with reticular dysgenesis 190996002

ancestors

sorted most to least specific

SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation 3439009
Disorder of immune structure 414030009
Hereditary white blood cell disorder 414395005
Congenital anemia 63565007
Congenital neutropenia 89655007
Severe combined immunodeficiency disease 31323000
Hemoglobin below reference range 165397008
Neutropenic disorder 303011007
Hereditary disorder of cellular element of blood 414393003
Red blood cell count below reference range 165423001
Anemia 271737000
Congenital immunodeficiency disease 36138009
Hereditary disorder of immune system 363138005
Hemoglobin level outside reference range 441793007
Quantitative disorder of neutrophils 105601003
Combined immunodeficiency disease 442459007
Red blood cell count outside reference range 165427000
Neutropenia 165517008
Leukopenia 84828003
Hereditary disorder by system 363137000
Hemoglobin finding 250220000
Quantitative abnormality of granulocytes 105602005
Congenital disease 66091009
Red blood cell count - finding 365625004
Hematology test outside reference range 34641000087106
Neutrophil count outside reference range 165519006
Granulocyte count below reference range 416955003
Disorder of body system 362965005
Hereditary disease 32895009
Hematopoietic system finding 106200001
Disorder of neutrophils 105600002
Protein level - finding 365799007
Blood leukocyte number below reference range 419188005
Disorder of phagocytic cell number 234574006
Genetic disease 782964007
White blood cell disorder 54097007
Finding of substance level 785671009
White blood cell count outside reference range 165509000
Phagocytic cell defect 234573000
Cytopenia 50820005
Disorder of cellular component of blood 414022008
Primary immune deficiency disorder 58606001
Measurement finding below reference range 442686002
White blood cell number - finding 365630000
Blood cell count outside reference range 762656009
Immunodeficiency disorder 234532001
Finding of blood, lymphatics and immune system 299691001
Measurement finding outside reference range 442096005
Disorder of immune function 414029004
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

Congenital immunodeficiency disease 36138009

Severe combined immunodeficiency disease 31323000

SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation 3439009

Severe combined immunodeficiency with reticular dysgenesis 190996002

SNOMED CT code