Immunodeficiency by defective expression of human leukocyte antigen class 1 725136003

SNOMED CT code

SNOMED code

725136003

name

Immunodeficiency by defective expression of human leukocyte antigen class 1

status

active

date introduced

2017-07-31

fully specified name(s)

Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)

synonyms

Immunodeficiency by defective expression of human leukocyte antigen class 1
Bare lymphocyte syndrome type 1
Bare lymphocyte syndrome type I
Immunodeficiency by defective expression of HLA (human leukocyte antigen) class 1
Immunodeficiency by defective expression of human leukocyte antigen class I

attributes - group3

Pathological process

Abnormal immune process 769247005

attributes - group1

Occurrence

Congenital 255399007

attributes - group2

Finding site

Body system structure 91689009

parents

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009

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
Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009
Immunodeficiency by defective expression of human leukocyte antigen class 1 725136003

ancestors

sorted most to least specific

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009
Severe combined immunodeficiency disease 31323000
Autosomal recessive hereditary disorder 85995004
Congenital immunodeficiency disease 36138009
Autosomal hereditary disorder 1899006
Hereditary disorder of immune system 363138005
Combined immunodeficiency disease 442459007
Hereditary disorder by system 363137000
Primary immune deficiency disorder 58606001
Congenital disease 66091009
Immunodeficiency disorder 234532001
Hereditary disease 32895009
Disorder of body system 362965005
Disorder of immune function 414029004
Genetic disease 782964007
Disease 64572001
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

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009

Immunodeficiency by defective expression of human leukocyte antigen class 1 725136003

SNOMED CT code