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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
amyloidosis +   
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.
carbohydrate metabolism disease +   
carotenemia +   
hyperprolactinemia +   
hyperuricemia +   
metabolic acidosis +   
mineral metabolism disease +   
nutrition disease +   
Reperfusion Injury +   
TDP-43 Proteinopathies +   

Synonyms
Exact Synonyms: Amyloidoses ;   amyloid disease
Related Synonyms: SERUM AMYLOID A VARIANT
Primary IDs: MESH:D000686 ;   RDO:0000040
Xrefs: ICD10CM:E85 ;   ICD9CM:277.3 ;   NCI:C2868
Definition Sources: https://en.wikipedia.org/wiki/Amyloidosis "DO", MESH:D000686

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.