SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Degenerative disorder  362975008

Amyloidosis  17602002

Hereditary amyloidosis  367601000119103

Localized hereditary amyloidosis   237869003

SNOMED CT code


SNOMED code237869003
nameLocalized hereditary amyloidosis
statusactive
date introduced2002-01-31
fully specified name(s)Localized hereditary amyloidosis (disorder)
synonyms
  • Organ limited hereditary amyloidosis
  • Localised hereditary amyloidosis
  • Localized hereditary amyloidosis
attributes - group1
Associated morphologyFocal amyloid   57174000
parents
children
  • Familial lichen amyloidosis   237870002
  • Hereditary cerebral hemorrhage with amyloidosis   724357007
  • Lattice corneal dystrophy   361199007
  • Localized hereditary cardiac amyloidosis   1187149000
  • Poikilodermal cutaneous amyloid   237872005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Hereditary amyloidosis   367601000119103
            Localized hereditary amyloidosis   237869003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Localized amyloidosis   56871000
            Localized hereditary amyloidosis   237869003

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

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