serw-MX  [xml]  
 


    
 DeCS Categories

C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.500 Amyloidosis .
C23 Pathological Conditions, Signs and Symptoms .
C23.300 Pathological Conditions, Anatomical .
C23.300.821 Plaque, Amyloid .
D05 Macromolecular Substances .
D05.500 Multiprotein Complexes .
D05.500.049 Amyloid .
D09 Carbohydrates .
D09.301 Dietary Carbohydrates .
D09.301.915 Starch .
D09.301.915.361 Amylose .
D09.698 Polysaccharides .
D09.698.365 Glucans .
D09.698.365.855 Starch .
D09.698.365.855.361 Amylose .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.049 Amyloid .
D12.776.049.407 Amyloidogenic Proteins .
D12.776.049.407.750 Serum Amyloid A Protein .
D12.776.124 Blood Proteins .
D12.776.124.050 Acute-Phase Proteins .
D12.776.124.050.725 Serum Amyloid A Protein .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Amyloid .
Amyloid Fibrils .
Amyloid Substance .
Fibrils, Amyloid .
Substance, Amyloid .
A fibrous protein complex that consists of proteins folded into a specific cross beta-pleated sheet structure. This fibrillar structure has been found as an alternative folding pattern for a variety of functional proteins. Deposits of amyloid in the form of AMYLOID PLAQUES are associated with a variety of degenerative diseases. The amyloid structure has also been found in a number of functional proteins that are unrelated to disease. .
1.00
3513131
 
Amyloidosis .
Amyloidoses .
A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. .
0.85
32117410
 
Amylose .
An unbranched glucan in starch. .
0.79
141690
 
Amyloidogenic Proteins .
Amyloid Proteins .
Proteins, Amyloid .
Proteins, Amyloidogenic .
Proteins that form the core of amyloid fibrils. For example, the core of amyloid A is formed from amyloid A protein, also known as serum amyloid A protein or SAA protein. .
0.79
2385
 
Plaque, Amyloid .
Amyloid Plaques .
Neuritic Plaques .
Senile Plaques .
Amyloid Deposit .
Amyloid Plaque .
Deposit, Amyloid .
Deposits, Amyloid .
Neuritic Plaque .
Plaque, Neuritic .
Plaque, Senile .
Plaques, Neuritic .
Plaques, Senile .
Senile Plaque .
Amyloid Deposits .
Plaques, Amyloid .
Amyloid Plaques .
Neuritic Plaques .
Senile Plaques .
Accumulations of extracellularly deposited AMYLOID FIBRILS within tissues. .
0.75
144021
 
Serum Amyloid A Protein .
Amyloid A Precursor .
Amyloid A Protein .
Amyloid A Protein-Related Serum Component .
Amyloid Fibril Protein AA .
Amyloid Protein AA .
Amyloid Protein AA Precursor .
Amyloid-Related Serum Protein (SAA) .
Serum Amyloid A .
Serum Amyloid Protein A .
Amyloid A Protein Related Serum Component .
Amyloid Protein SAA .
Amyloid Serum Protein SAA .
Serum A Related Protein .
Protein AA .
Serum Amyloid Protein A .
Amyloid Protein AA .
Amyloid A Protein .
Amyloid Fibril Protein AA .
An ACUTE PHASE REACTION protein present in low concentrations in normal sera, but found at higher concentrations in sera of older persons and in patients with AMYLOIDOSIS. It is the circulating precusor of amyloid A protein, which is found deposited in AA type AMYLOID FIBRILS. .
0.74
243538