Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency 725151007

SNOMED CT code

SNOMED code

725151007

name

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency

status

active

date introduced

2017-07-31

fully specified name(s)

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)

synonyms

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency

attributes - group2

Pathological process

Abnormal immune process 769247005

parents

Autosomal dominant hereditary disorder 11164009
Mendelian susceptibility to mycobacterial disease 1172895006

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency 725151007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Mendelian susceptibility to mycobacterial disease 1172895006
Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency 725151007

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Mendelian susceptibility to mycobacterial disease 1172895006
Autosomal hereditary disorder 1899006
Primary immune deficiency disorder 58606001
Hereditary disease 32895009
Immunodeficiency disorder 234532001
Genetic disease 782964007
Disorder of immune function 414029004
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency 725151007

SNOMED CT code