Congenital anomaly  107656002

Developmental anomaly  21390004

Congenital anomaly   107656002

SNOMED CT code


SNOMED code107656002
nameCongenital anomaly
statusremoved
date introduced2002-01-31
date removed2019-01-31
fully specified name(s)Congenital anomaly (morphologic abnormality)
synonymsCongenital anomaly
parentsDevelopmental anomaly   21390004  removed: 2021-07-31
children
  • Congenital abnormal communication   74175007  removed: 2002-07-31
  • Congenital contracture   91287001  removed: 2014-07-31
  • Congenital deficiency   43451003  removed: 2014-07-31
  • Congenital degeneration   64464000  removed: 2014-07-31
  • Congenital developmental anomaly   371519002  removed: 2014-07-31
  • Congenital dystrophy   71514005  removed: 2014-07-31
  • Congenital fistula   40086006  removed: 2019-07-31
  • Congenital hypoplasia   38146002  removed: 2019-01-31
  • Congenital impairment   58404005  removed: 2014-07-31
  • Congenital incomplete closure   8352002  removed: 2003-07-31
  • Congenital malformation   112635002  removed: 2014-07-31
  • Developmental anomaly   21390004  removed: 2021-07-31
  • Multiple congenital anomalies   67024003  removed: 2014-07-31
hierarchies
a selection of possible paths
Congenital anomaly   107656002  removed: 2019-01-31
  Developmental anomaly   21390004  removed: 2021-07-31
    Congenital anomaly   107656002  removed: 2019-01-31

ancestors
sorted most to least specific
  • Developmental anomaly   21390004  removed: 2021-07-31
  • Congenital anomaly   107656002  removed: 2019-01-31
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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