Lichtenstein syndrome 763668009
SNOMED CT code
SNOMED code | 763668009 |
---|---|
name | Lichtenstein syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Lichtenstein syndrome (disorder) |
synonyms | Lichtenstein syndrome |
attributes - group2 | |
Pathological process | Abnormal immune process 769247005 |
attributes - group1 | |
Finding site | Immune system structure 116003000 |
Occurrence | Congenital 255399007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Phagocytic cell defect 234573000 Phagocytic cell dysfunction 302874002 Lichtenstein syndrome 763668009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Lichtenstein syndrome 763668009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Lichtenstein syndrome 763668009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of immune structure 414030009 Lichtenstein syndrome 763668009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Lichtenstein syndrome 763668009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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