Terminology Service for NFDI4Health

amyloidosis

Go to external page http://www.ebi.ac.uk/efo/EFO_1001875


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. [ ]

Term info

Label

amyloidosis

Synonyms
  • amyloid
  • amyloid disease
  • amyloidoses
  • amyloidosis
  • amyloidosis (disease)
  • systemic amyloidosis
database cross reference
Subsets

disease_grouping, ordo_group_of_disorders

IAO 0000589

amyloidosis (disease)

broadMatch

https://icd.codes/icd10cm/E85.0, https://icd.codes/icd10cm/E85.1, https://icd.codes/icd10cm/E85.2, https://icd.codes/icd10cm/E85.3, https://icd.codes/icd10cm/E85.8, https://icd.codes/icd10cm/E85.9, https://icd.codes/icd10cm/E85.4

closeMatch

http://identifiers.org/meddra/10002022

exactMatch

http://purl.obolibrary.org/obo/DOID_9120, http://identifiers.org/mesh/D000686, http://purl.obolibrary.org/obo/NCIT_C2868, http://identifiers.org/snomedct/17602002, http://linkedlifedata.com/resource/umls/id/C0002726, http://purl.obolibrary.org/obo/Orphanet_69

id

EFO:1001875

term editor

Gautier Koscielny