Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007
SNOMED CT code
| SNOMED code | 1279887007 |
|---|---|
| name | Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome |
| status | active |
| date introduced | 2023-04-30 |
| fully specified name(s) | Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome (disorder) |
| synonyms |
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| attributes - group3 | |
| Due to | Decay accelerating factor deficiency 234624002 |
| attributes - group2 | |
| Finding site | Small intestinal structure 30315005 |
| attributes - group1 | |
| Finding site | Immune system structure 116003000 |
| Pathological process | Abnormal immune process 769247005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of immune structure 414030009 Complement regulatory factor defect 234618008 Decay accelerating factor deficiency 234624002 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Gastrointestinal complication 24813008 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Malabsorption syndrome 32230006 Protein-losing enteropathy 66972006 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome 1279887007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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