" /> Amyloidosis - CISMeF





ICD-11 code : 5D00;

Preferred Label : Amyloidosis;

ICD-11 definition : Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clinical signs and biochemical type of amyloid protein involved. Most amyloidoses are multisystemic, 'generalized' or 'diffuse'. There are a few forms of localized amylosis. The most frequent forms are AL amyloidosis (immunoglobulins), AA (inflammatory), and ATTR (transthyretin accumulation).;

ICD-11 synonym : idiopathic amyloidosis; amyloid infiltration; amyloid; lardaceous degeneration; amyloid degeneration; hyaloid degeneration; amyloid disease; amyloid deposition; amyloidosis NOS;

ICD-11 "other" category code : 5D00.Y;

ICD-11 "unspecified" category code : 5D00.Z;

Détails


Position du mot-clé dans l'(les) arborescence(s) : arborescence

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Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clinical signs and biochemical type of amyloid protein involved. Most amyloidoses are multisystemic, 'generalized' or 'diffuse'. There are a few forms of localized amylosis. The most frequent forms are AL amyloidosis (immunoglobulins), AA (inflammatory), and ATTR (transthyretin accumulation).

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31/07/2025


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