familiaire neuropathische amyloïdose

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familiaire amyloïdneuropathie type I (aandoening)
	familiaire amyloïdneuropathie type I
	Dit betekent dat bepaalde stoffen zich ophopen in je zenuwen. Daarom kun je pijn, gevoelloosheid of tintelingen krijgen. Dit kan vaker voorkomen in je familie.
	Amyloid polyneuropathy type I
	Portuguese polyneuritic amyloidosis Familial amyloid polyneuropathy, 30 Met-for-Val Corino de Andrade paramyloidosis Hereditary amyloid polyneuropathy Portuguese type Portuguese type amyloid polyneuropathy Hereditary neuropathic amyloidosis, type I Familial amyloid neuropathy, Andrade type Andrade syndrome Familial amyloid neuropathy, Portuguese type Swedish type amyloid polyneuropathy Japanese type amyloid polyneuropathy Amyloidosis, type I Andrade type amyloid polyneuropathy Wohlwill-Corino Andrade syndrome

Id	398229007
Status	Primitive

Associated morphology	depositie van amyloïd
Finding site	structuur van perifere zenuw

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E85.1
Term	Neuropathische heredofamiliale amyloïdose

SNOMED CT to ICD-10 extended map

Target	E85.1
Rule	TRUE
Advice	ALWAYS E85.1
Correlation	SNOMED CT source code to target map code correlation not specified

Target	G63.3
Rule	TRUE
Advice	ALWAYS G63.3 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
Correlation	SNOMED CT source code to target map code correlation not specified