AGel amyloidosis   783160006

SNOMED CT code


SNOMED code783160006
nameAGel amyloidosis
statusactive
date introduced2019-07-31
fully specified name(s)Hereditary gelsolin amyloidosis (disorder)
synonyms
  • Hereditary gelsolin amyloidosis
  • Familial amyloidosis Finnish type
  • AGel amyloidosis
  • Hereditary amyloidosis Finnish type
  • Familial amyloid polyneuropathy type IV
  • Gelsolin amyloidosis
  • Lattice corneal dystrophy type II
attributes - group4
Associated morphologyAmyloid deposition   68790008
Finding siteEye structure   81745001
attributes - group3
Finding siteNervous system structure   25087005
Associated morphologyAmyloid deposition   68790008
attributes - group1
Finding siteCorneal structure   28726007
Associated morphologyDystrophy   4720007
attributes - group2
Associated morphologyFocal amyloid   57174000
Finding siteSkin structure   39937001
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Hereditary amyloidosis   367601000119103
            AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Systemic disease   56019007
        Systemic disease affecting skin   238980001
          Systemic amyloidosis affecting skin   402719006
            AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary corneal dystrophy   77797009
            AGel amyloidosis   783160006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Ocular amyloid deposit   8231007
            AGel amyloidosis   783160006

ancestors
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