SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Congenital dystrophia brevicollis   129581007

SNOMED CT code


SNOMED code129581007
nameCongenital dystrophia brevicollis
statusremoved
date introduced2002-01-31
date removed2003-01-31
fully specified name(s)Congenital dystrophia brevicollis (disorder)
synonyms
  • Congenital dystrophia brevicollis
  • Bonnevie-Ullrich and Klippel-Feil syndrome
  • Klippel-Feil and Turner syndrome
  • Nielsen's disease
parentsAutosomal hereditary disorder   1899006
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
            Congenital dystrophia brevicollis   129581007  removed: 2003-01-31

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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