AL Amyloidosis is a plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor. It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA) restricted to a single organ. [ Orphanet:85443 ]

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:C531616 (Orphanet:85443)
  • Orphanet:85443 (MONDO:equivalentTo)
  • MedDRA:10036673 (Orphanet:85443)
  • ICD10:E85.9 (Orphanet:85443)
  • GARD:0005797 (MONDO:equivalentTo)
  • UMLS:C0268381 (Orphanet:85443)
Subsets

gard_rare, ordo_disease

definition

AL Amyloidosis is a plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor. It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA) restricted to a single organ.

exactMatch

http://identifiers.org/meddra/10036673

http://linkedlifedata.com/resource/umls/id/C0268381

http://www.orpha.net/ORDO/Orphanet_85443

http://identifiers.org/mesh/C531616

has exact synonym

primary amyloidosis

Light-chain amyloidosis

has related synonym

amyloidosis AL

amyloidosis primary systemic

primary amyloidosis (formerly)

primary systemic AL amyloidosis

Light chain amyloidosis

primary systemic amyloidosis

primary AL amyloidosis

systemic AL amyloidsis

id

MONDO:0019438