Autosomal dominant Charcot-Marie-Tooth disease type 2O 782829002
SNOMED CT code
| SNOMED code | 782829002 |
|---|---|
| name | Autosomal dominant Charcot-Marie-Tooth disease type 2O |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Autosomal dominant Charcot-Marie-Tooth disease type 2O (disorder) |
| synonyms | Autosomal dominant Charcot-Marie-Tooth disease type 2O |
| attributes - group1 | |
| Occurrence | Early childhood 713152004 |
| Finding site | Nerve structure 3057000 |
| Associated morphology | Atrophy 13331008 |
| attributes - group2 | |
| Occurrence | Early childhood 713152004 |
| Finding site | Peripheral nervous system structure 3058005 |
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Charcot-Marie-Tooth disease, type II 398187000 Autosomal dominant Charcot-Marie-Tooth disease type 2 1156835005 Autosomal dominant Charcot-Marie-Tooth disease type 2O 782829002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Autosomal dominant Charcot-Marie-Tooth disease type 2O 782829002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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