Congenital end-plate acetylcholine receptor deficiency 230673001
SNOMED CT code
SNOMED code | 230673001 |
---|---|
name | Congenital end-plate acetylcholine receptor deficiency |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital end-plate acetylcholine receptor deficiency (disorder) |
synonyms | Congenital end-plate acetylcholine receptor deficiency |
attributes - group1 | |
Finding site | Neuromuscular junction 31627007 |
Pathological process | Autoimmune process 263680009 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Finding site | Skeletal muscle structure 127954009 |
attributes - group3 | |
Pathological process | Hypersensitivity process 472963003 |
parents | Congenital myasthenic syndrome 230672006 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital myasthenic syndrome 230672006 Congenital end-plate acetylcholine receptor deficiency 230673001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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