Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000
SNOMED CT code
| SNOMED code | 1197594000 |
|---|---|
| name | Periodic fever, infantile enterocolitis, autoinflammatory syndrome |
| status | active |
| date introduced | 2022-02-28 |
| fully specified name(s) | Periodic fever, infantile enterocolitis, autoinflammatory syndrome (disorder) |
| synonyms |
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| attributes - group4 | |
| Clinical course | Recurrent 255227004 |
| attributes - group5 | |
| Associated with | Fever 386661006 |
| attributes - group2 | |
| Occurrence | Infancy 3658006 |
| Finding site | Small intestinal structure 30315005 |
| Associated morphology | Inflammatory morphology 409774005 |
| attributes - group3 | |
| Occurrence | Infancy 3658006 |
| Finding site | Colon structure 71854001 |
| Associated morphology | Inflammatory morphology 409774005 |
| attributes - group1 | |
| Finding site | Mononuclear phagocyte system structure 127908000 |
| Associated morphology | Histiocytic proliferation 1186648002 |
| Pathological process | Abnormal immune process 769247005 |
| attributes - group6 | |
| Interprets | Body temperature 386725007 |
| Has interpretation | Above reference range 281302008 |
| attributes - group7 | |
| 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 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Recurrent disease 58184002 Hereditary periodic fever 402790006 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of blood, lymphatics and immune system 299691001 Disorder of cellular component of blood 414022008 White blood cell disorder 54097007 Hereditary white blood cell disorder 414395005 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of hematopoietic structure 414027002 Hemophagocytic lymphohistiocytosis 234437005 Macrophage activation syndrome 430478003 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Finding of small intestine 118435004 Disorder of small intestine 119522002 Enteritis of small intestine 64613007 Enterocolitis 43752006 Periodic fever, infantile enterocolitis, autoinflammatory syndrome 1197594000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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