Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

SNOMED CT code

SNOMED code

234571003

name

Warts, hypogammaglobulinemia, infections, and myelokathexis

status

active

date introduced

2002-01-31

fully specified name(s)

Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)

synonyms

WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis
WHIM - Warts, hypogammaglobulinemia, infections and myelokathexis
Warts, hypogammaglobulinaemia, infections, and myelokathexis
Warts, hypogammaglobulinemia, infections, and myelokathexis

attributes - group2

Interprets

Neutrophil count 30630007

Has interpretation

Below reference range 281300000

attributes - group1

Finding site

Immune system structure 116003000

Pathological process

Abnormal immune process 769247005

Occurrence

Congenital 255399007

parents

Myelokathexis 24974008
Severe combined immunodeficiency disease 31323000
Disorder of immune structure 414030009
Hereditary white blood cell disorder 414395005
Congenital neutropenia 89655007

hierarchies

a selection of possible paths

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
Leukopenia 84828003
Neutropenic disorder 303011007
Myelokathexis 24974008
Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital immunodeficiency disease 36138009
Severe combined immunodeficiency disease 31323000
Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of immune structure 414030009
Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

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
Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital immunodeficiency disease 36138009
Congenital neutropenia 89655007
Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

ancestors

sorted most to least specific

Myelokathexis 24974008
Severe combined immunodeficiency disease 31323000
Disorder of immune structure 414030009
Hereditary white blood cell disorder 414395005
Congenital neutropenia 89655007
Neutropenic disorder 303011007
Congenital immunodeficiency disease 36138009
Hereditary disorder of immune system 363138005
Combined immunodeficiency disease 442459007
Hereditary disorder of cellular element of blood 414393003
Quantitative disorder of neutrophils 105601003
Hereditary disorder by system 363137000
Neutropenia 165517008
Leukopenia 84828003
Congenital disease 66091009
Quantitative abnormality of granulocytes 105602005
Disorder of body system 362965005
Hereditary disease 32895009
Neutrophil count outside reference range 165519006
Granulocyte count below reference range 416955003
Disorder of neutrophils 105600002
Genetic disease 782964007
Blood leukocyte number below reference range 419188005
Disorder of phagocytic cell number 234574006
White blood cell disorder 54097007
White blood cell count outside reference range 165509000
Phagocytic cell defect 234573000
Cytopenia 50820005
Disorder of cellular component of blood 414022008
White blood cell number - finding 365630000
Primary immune deficiency disorder 58606001
Blood cell count outside reference range 762656009
Measurement finding below reference range 442686002
Finding of blood, lymphatics and immune system 299691001
Immunodeficiency disorder 234532001
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

Finding of blood, lymphatics and immune system 299691001

Disorder of cellular component of blood 414022008

White blood cell disorder 54097007

Leukopenia 84828003

Neutropenic disorder 303011007

Myelokathexis 24974008

Warts, hypogammaglobulinemia, infections, and myelokathexis 234571003

SNOMED CT code