Amyloidosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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, 'generalised' or 'diffuse'. There are a few forms of localised amylosis. The most frequent forms are AL amyloidosis (immunoglobulins), AA (inflammatory), and ATTR (transthyretin accumulation).
exclusions
sections/codes in this section (5D00-5D00)
- AL amyloidosis (5D00.0)
- AA amyloidosis (5D00.1)
- Hereditary amyloidosis (5D00.2)
- Dialysis-associated amyloidosis (5D00.3)
- Other specified amyloidosis (5D00.Y)
- Amyloidosis, unspecified (5D00.Z)
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