Vasculitis due to adenosine deaminase 2 deficiency 770687001
SNOMED CT code
| SNOMED code | 770687001 |
|---|---|
| name | Vasculitis due to adenosine deaminase 2 deficiency |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Vasculitis due to adenosine deaminase 2 deficiency (disorder) |
| synonyms |
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| attributes - group2 | |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group1 | |
| Associated morphology | Inflammatory morphology 409774005 |
| Finding site | Vascular structure 59820001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 General finding of soft tissue 248402002 Disorder of soft tissue 19660004 Vascular disorder 27550009 Vasculitis 31996006 Vasculitis due to adenosine deaminase 2 deficiency 770687001 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Vasculitis due to adenosine deaminase 2 deficiency 770687001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Vasculitis due to adenosine deaminase 2 deficiency 770687001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Vasculitis due to adenosine deaminase 2 deficiency 770687001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Vasculitis due to adenosine deaminase 2 deficiency 770687001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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