8C01.3 Chronic inflammatory demyelinating polyneuropathy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Chronic inflammatory demyelinating polyneuropathy is a chronic monophasic, progressive or relapsing symmetric sensorimotor disorder characterised by progressive muscular weakness with impaired sensation, absent or diminished tendon reflexes and elevated cerebrospinal fluid proteins.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Chronic inflammatory demyelinating polyneuropathy
- Multifocal motor neuropathy with persistent conduction block
- Sensory predominant chronic inflammatory demyelinating neuropathy
- Distal acquired demyelinating sensory neuropathy associated with IgM paraprotein
- Chronic inflammatory demyelinating neuropathy with central nervous involvement
- Progressive chronic inflammatory demyelinating neuropathy
- Relapsing remitting chronic inflammatory demyelinating neuropathy
- Multifocal motor or sensory demyelinating mononeuropathy
- Lewis-Sumner syndrome
- CANOMAD - [Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies] syndrome
- Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies
- Chronic ataxic neuropathy - ophthalmoplegia - IgM paraprotein - cold agglutinins - disialosyl antibodies
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