SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Developmental hereditary disorder  363070008

Atelosteogenesis  43814000

Omodysplasia I   254056003

SNOMED CT code


SNOMED code254056003
nameOmodysplasia I
statusremoved
date introduced2002-01-31
date removed2017-07-31
fully specified name(s)Omodysplasia I (disorder)
synonyms
  • Omodysplasia, Maroteaux type
  • Omodysplasia I
parentsAtelosteogenesis   43814000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Atelosteogenesis   43814000
            Omodysplasia I   254056003  removed: 2017-07-31

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:
  • CPT® to SNOMED Crosswalks

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