Congenital neuropathy with arthrogryposis multiplex congenita 230561007
SNOMED CT code
| SNOMED code | 230561007 | ||
|---|---|---|---|
| name | Congenital neuropathy with arthrogryposis multiplex congenita | ||
| status | active | ||
| date introduced | 2002-01-31 | ||
| fully specified name(s) | Congenital neuropathy with arthrogryposis multiplex congenita (disorder) | ||
| synonyms | Congenital neuropathy with arthrogryposis multiplex congenita | ||
| attributes - group1 | |||
| Occurrence | Congenital 255399007 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Nerve structure 3057000 | ||
| attributes - group2 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Finding site | Structure of joint region 785818007 | ||
| Occurrence | Congenital 255399007 | ||
| Associated morphology | Contracture 57048009 | ||
| attributes - group3 | |||
| Interprets | Range of joint movement 364564000 | ||
| Has interpretation | Decreased 1250004 | ||
| parents | |||
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Congenital neuropathy with arthrogryposis multiplex congenita 230561007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of body system 362965005 Disorder of nervous system 118940003 Neuropathy 386033004 Congenital neuropathy with arthrogryposis multiplex congenita 230561007 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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