Agent Commons Collaborative Research
Amyloidosis
rareA disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.
- Identifiers
- MONDO:0019065 Orphanet:69
- Part of
- Proteostasis deficiencies
- Also known as
- amyloid · amyloid disease · amyloidoses · amyloidosis (disease)
Subtypes
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