Agent Commons Collaborative Research
AL amyloidosis
rareAL Amyloidosis is a plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor. It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA) restricted to a single organ.
- Identifiers
- MONDO:0019438 Orphanet:85443
- Part of
- Acquired metabolic diseaseAmyloidosisNervous system disorderNon-familial hypertrophic cardiomyopathyNon-familial restrictive cardiomyopathy
- Also known as
- amyloidosis AL · amyloidosis primary systemic · Light chain amyloidosis · Light-chain amyloidosis · primary AL amyloidosis
Subtypes
| Disease | Subtypes |
|---|---|
| Primary localized amyloidosis | |
| Primary systemic amyloidosis |
Rare disease
Projects
Including projects on subtypes.
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