Putative defect in acetylcholine synthesis or packaging 230676009
SNOMED CT code
SNOMED code | 230676009 |
---|---|
name | Putative defect in acetylcholine synthesis or packaging |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Putative defect in acetylcholine synthesis or packaging (disorder) |
synonyms | Putative defect in acetylcholine synthesis or packaging |
attributes - group1 | |
Finding site | Neuromuscular junction 31627007 |
Pathological process | Autoimmune process 263680009 |
attributes - group3 | |
Pathological process | Hypersensitivity process 472963003 |
attributes - group2 | |
Finding site | Skeletal muscle structure 127954009 |
parents | Genetically determined myasthenia 230669004 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Genetically determined myasthenia 230669004 Putative defect in acetylcholine synthesis or packaging 230676009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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