Combined immunodeficiency, enteropathy spectrum 1197428008
SNOMED CT code
| SNOMED code | 1197428008 |
|---|---|
| name | Combined immunodeficiency, enteropathy spectrum |
| status | active |
| date introduced | 2022-02-28 |
| fully specified name(s) | Combined immunodeficiency, enteropathy spectrum (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Intestinal structure 113276009 |
| Associated morphology | Congenital atresia 56457002 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Finding site | Intestinal structure 113276009 |
| Associated morphology | Inflammatory morphology 409774005 |
| Pathological process | Dysregulated host response 769256002 |
| attributes - group3 | |
| Interprets | Lymphocyte count 74765001 |
| Has interpretation | Below reference range 281300000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Inflammatory disorder 128139000 Inflammation of specific body structures or tissue 363170005 Inflammation of specific body organs 363169009 Enteritis of intestine 1187638005 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Inflammatory disorder 128139000 Inflammatory bowel disease 24526004 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Combined immunodeficiency, enteropathy spectrum 1197428008 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 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Combined immunodeficiency disease 442459007 Combined immunodeficiency, enteropathy spectrum 1197428008 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 Lymphocyte disorder 3239007 Lymphocytopenia 48813009 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Combined immunodeficiency, enteropathy spectrum 1197428008 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Bowel finding 249562008 Disorder of intestine 85919009 Congenital anomaly of intestinal tract 126764002 Congenital atresia of intestinal tract 93032003 Combined immunodeficiency, enteropathy spectrum 1197428008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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