Déjérine-Sottas disease 111499002
SNOMED CT code
SNOMED code | 111499002 |
---|---|
name | Déjérine-Sottas disease |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Déjérine-Sottas disease (disorder) |
synonyms |
|
attributes - group1 | |
Finding site | Peripheral nerve structure 84782009 |
Associated morphology | Remyelination 30321009 |
attributes - group2 | |
Finding site | Peripheral nerve structure 84782009 |
Associated morphology | Hypertrophy 56246009 |
attributes - group3 | |
Finding site | Peripheral nerve structure 84782009 |
Associated morphology | Segmental demyelination 8723003 |
parents | |
children | Roussy-Levy syndrome 307540002 removed: 2009-07-31 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Peripheral demyelinating neuropathy 23414001 Hypertrophic interstitial neuropathy 18708008 Déjérine-Sottas disease 111499002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hereditary peripheral neuropathy 65017003 Hereditary motor and sensory neuropathy 398100001 Déjérine-Sottas disease 111499002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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