AL amyloidosis   23132008

SNOMED CT code


SNOMED code23132008
nameAL amyloidosis
statusactive
date introduced2002-01-31
fully specified name(s)Amyloid light-chain amyloidosis (disorder)
synonyms
  • Amyloid light-chain amyloidosis
  • Primary amyloidosis of light chain type
  • AL amyloidosis
attributes - group5
Pathological processAbnormal immune process   769247005
attributes - group4
Causative agentImmunoglobulin, light chain   87316007
Associated morphologyAmyloid deposition   68790008
attributes - group3
Has interpretationDetected   260373001
InterpretsParaprotein measurement   250174000
attributes - group1
Has interpretationAbove reference range   281302008
InterpretsSerum globulin measurement   270994009
attributes - group2
Has interpretationAbove reference range   281302008
InterpretsImmunoglobulin measurement   42441008
parents
children
  • Amyloid light chain amyloidosis due to multiple myeloma   402453006
  • Amyloid light-chain nephropathy   426598005
  • Primary amyloidosis of light chain type   237865009  removed: 2020-01-31
  • Primary systemic amyloidosis associated with occult plasma cell dyscrasia   402454000
  • Sporadic primary amyloidosis   190923000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          AL amyloidosis   23132008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of immune function   414029004
        Gammopathy   111001004
          Immunosecretory disorder   414031008
            Monoclonal gammopathy (clinical)   109983007
              Light chain disease   51319002
                AL amyloidosis   23132008

ancestors
sorted most to least specific
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