You are using an outdated browser. Please upgrade your browser to improve your experience.
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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
COHD:432595
DOID:9120
EFO:1001875
ICD9:277.3
ICD9:277.30
MESH:D000686
NCIT:C2868
ONCOTREE:MIDDA
Orphanet:69
SCTID:17602002
UMLS:C0002726
MONDO:0019065
High level summary of knowledge for a disease, including descriptions and datasource references.