Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency 1197361002
SNOMED CT code
SNOMED code | 1197361002 |
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name | Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency |
status | active |
date introduced | 2022-02-28 |
fully specified name(s) | Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Lymphocyte 56972008 |
Associated morphology | Lymphoproliferative disorder 414629003 |
Pathological process | Autoimmune process 263680009 |
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 Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency 1197361002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of hematopoietic morphology 414026006 Lymphoproliferative disorder 277466009 Autoimmune lymphoproliferative syndrome 702444009 Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency 1197361002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Autoimmune disease 85828009 Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency 1197361002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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