SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Chromosomal disorder  409709004

Extra unidentified structurally abnormal chromosome  444655009

Familial extra unidentified structurally abnormal chromosome   445580008

SNOMED CT code


SNOMED code445580008
nameFamilial extra unidentified structurally abnormal chromosome
statusactive
date introduced2010-07-31
fully specified name(s)Familial extra unidentified structurally abnormal chromosome (disorder)
synonyms
  • Familial extra unidentified structurally abnormal chromosome
  • Familial marker chromosome
attributes - group1
Finding siteChromosome structure   312237004
parentsExtra unidentified structurally abnormal chromosome   444655009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Extra unidentified structurally abnormal chromosome   444655009
          Familial extra unidentified structurally abnormal chromosome   445580008

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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