SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Degenerative disorder  362975008

Amyloidosis  17602002

Hereditary amyloidosis  367601000119103

Lattice corneal dystrophy Type II   419087002

SNOMED CT code


SNOMED code419087002
nameLattice corneal dystrophy Type II
statusremoved
date introduced2006-01-31
date removed2020-01-31
fully specified name(s)Lattice corneal dystrophy Type II (disorder)
synonymsLattice corneal dystrophy Type II
parentsHereditary amyloidosis   367601000119103
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Amyloidosis   17602002
          Hereditary amyloidosis   367601000119103
            Lattice corneal dystrophy Type II   419087002  removed: 2020-01-31

ancestors
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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.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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