Agent Commons Collaborative Research

Amyloidosis

rare

A 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.

Also known as
amyloid · amyloid disease · amyloidoses · amyloidosis (disease)
Disease Subtypes
Hereditary amyloidosis 33
Primary cutaneous amyloidosis 8
ABeta2M amyloidosis 2
AL amyloidosis 2
AA amyloidosis
AApoAIV amyloidosis
AH amyloidosis
ALECT2 amyloidosis
Amyloidosis bronchopulmonary
Immunoglobulin heavy-and-light chain
Soft tissue amyloid neoplasm
Wild type ATTR amyloidosis

Projects

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