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amyloidosis

Disease Summary
Associated Targets (60)
Tbio

39

Tchem

11

Tclin

10


Mondo Description 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.
Disease Ontology Description An acquired metabolic disease that has_material_basis_in extracellular tissue deposition of mis-folded proteins called fibrils composed of low molecular weight subunits of a variety of proteins. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition.
Mondo Term and Equivalent IDs
MONDO:0019065:  amyloidosis
COHD:432595: 
EFO:1001875: 
ICD9:277.3: 
ICD9:277.30: 
MESH:D000686: 
NCIT:C2868: 
ONCOTREE:MIDDA: 
Orphanet:69: 
SCTID:17602002: 
UMLS:C0002726: