SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Chromosomal disorder  409709004

Congenital chromosomal disease  74345006

Other condition due to autosomal anomaly   205645002

SNOMED CT code


SNOMED code205645002
nameOther condition due to autosomal anomaly
statusremoved
date introduced2002-01-31
date removed2010-01-31
fully specified name(s)Other condition due to autosomal anomaly (disorder)
synonymsOther condition due to autosomal anomaly
parentsCongenital chromosomal disease   74345006
children
  • Conditions due to anomaly of unspecified chromosome NOS   205729005  removed: 2010-01-31
  • Other specified conditions due to autosomal anomalies   268296004  removed: 2010-01-31
  • Unspecified conditions due to autosomal anomalies   268297008  removed: 2010-01-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Other condition due to autosomal anomaly   205645002  removed: 2010-01-31

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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