SNOMED CT Concept  138875005

Clinical finding  404684003

Eye / vision finding  118235002

Visual system disorder  128127008

Hereditary disorder of the visual system  363343008

Hereditary retinal dystrophy  41799005

Pigmentary retinal dystrophy   68222009

SNOMED CT code


SNOMED code68222009
namePigmentary retinal dystrophy
statusremoved
date introduced2002-01-31
date removed2018-07-31
fully specified name(s)Pigmentary retinal dystrophy (disorder)
synonyms
  • Pigmentary retinal dystrophy
  • Albipunctate retinal dystrophy
  • Lauber's disease
  • Fundus albipunctatus
parentsHereditary retinal dystrophy   41799005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary retinal dystrophy   41799005
            Pigmentary retinal dystrophy   68222009  removed: 2018-07-31

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.

Access to this feature is available in the following products:
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