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amyloidosis

Go to external page http://purl.obolibrary.org/obo/DOID_9120

A disease of metabolism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition. [ http://purl.obolibrary.org/obo/ECO_0007638 url:https://www.tandfonline.com/doi/pdf/10.1080/13506129.2020.1835263?needAccess=true url:https://pubmed.ncbi.nlm.nih.gov/33100054/ url:https://en.wikipedia.org/wiki/Amyloidosis url:https://pubmed.ncbi.nlm.nih.gov/33787033/ ]

Synonyms: amyloid disease

This is just here as a test because I lose it

Term information

database cross reference
  • NCI:C2868
  • ICD9CM:277.3
  • MESH:D000686
  • UMLS_CUI:C0002726
  • SNOMEDCT_US_2023_03_01:154769007
  • ICD10CM:E85
Subsets

DO_MGI_slim, DO_FlyBase_slim, NCIthesaurus

comment

amyloidosis has both inherited and acquired subtypes [LS].

has exact match

MESH:D000686

has obo namespace

disease_ontology

id

DOID:9120

Term relations

Subclass of: