Ulnar mammary syndrome   700211007

SNOMED CT code


SNOMED code700211007
nameUlnar mammary syndrome
statusactive
date introduced2014-07-31
fully specified name(s)Ulnar mammary syndrome (disorder)
synonyms
  • Ulnar mammary syndrome
  • Ulnar-mammary syndrome
  • Schinzel syndrome
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyCellular AND/OR subcellular abnormality   107673000
Finding siteChromosome pair 12   17897000
parents
  • Autosomal dominant hereditary disorder   11164009
  • Anomaly of chromosome pair 12   37535007
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
            Autosomal dominant hereditary disorder   11164009
              Ulnar mammary syndrome   700211007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Anomaly of chromosome pair   362984008
            Anomaly of chromosome pair 12   37535007
              Ulnar mammary syndrome   700211007

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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.