Deficiency of interleukin 36 receptor antagonist 784339002
SNOMED CT code
| SNOMED code | 784339002 |
|---|---|
| name | Deficiency of interleukin 36 receptor antagonist |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Deficiency of interleukin 36 receptor antagonist (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Abnormal immune process 769247005 |
| Associated morphology | Inflammatory morphology 409774005 |
| Finding site | Skin structure 39937001 |
| attributes - group1 | |
| Finding site | Skin structure 39937001 |
| Pathological process | Hypersensitivity process 472963003 |
| Associated morphology | Vesiculobullous rash 14912003 |
| attributes - group3 | |
| Clinical course | Recurrent acute 255228009 |
| attributes - group4 | |
| Finding site | Immune system structure 116003000 |
| Associated morphology | Inflammatory morphology 409774005 |
| Pathological process | Abnormal immune process 769247005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Generalized pustular psoriasis 238612002 Deficiency of interleukin 36 receptor antagonist 784339002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Deficiency of interleukin 36 receptor antagonist 784339002 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Deficiency of interleukin 36 receptor antagonist 784339002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Autoinflammatory disease 42111000175103 Deficiency of interleukin 36 receptor antagonist 784339002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Deficiency of interleukin 36 receptor antagonist 784339002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Deficiency of interleukin 36 receptor antagonist 784339002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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