Chronic inflammatory demyelinating polyradiculoneuropathy

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Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome (disorder)
	CANOMAD syndrome
	Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome CANOMAD (chronic ataxic neuropathy, ophthalmoplegia, monoclonal IgM protein, cold agglutinins and disialosyl antibodies) syndrome Chronic ataxic neuropathy, ophthalmoplegia, monoclonal IgM protein, cold agglutinins and disialosyl antibodies
	A rare chronic immune-mediated demyelinating polyneuropathy. The exact prevalence is unknown but less than 30 cases have been reported in the literature. The clinical picture comprises a chronic neuropathy with marked sensory ataxia and areflexia, and with relatively preserved motor function in the limbs. Motor weakness affecting the oculomotor and bulbar muscles is present as either a fixed or relapsing-remitting feature.
	syndroom van chronische atactische neuropathie, oftalmoplegie, monoklonale immunoglobuline M, koudeagglutinine en disialosyl antistoffen
	CANOMAD-syndroom syndroom van chronische atactische neuropathie, oftalmoplegie, monoklonale IgM, koudeagglutinine en disialosyl antistoffen

Id	715624006
Status	Primitive

Clinical course

Associated morphology	Inflammatory morphology
Finding site	Peripheral nerve structure

Associated morphology	Demyelination
Finding site	Peripheral nerve structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G61.8
Rule	TRUE
Advice	ALWAYS G61.8
Correlation	SNOMED CT source code to target map code correlation not specified