Congenital anomaly of cardiovascular system   9904008

SNOMED CT code


SNOMED code9904008
nameCongenital anomaly of cardiovascular system
statusactive
date introduced2002-01-31
fully specified name(s)Congenital anomaly of cardiovascular system (disorder)
synonymsCongenital anomaly of cardiovascular system
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteCardiovascular structure   113257007
parents
children
  • [X]Congenital malformations of the circulatory system   205871000  removed: 2009-01-31
  • Brachydactyly, mesomelia, intellectual disability, heart defect syndrome   765761009
  • Congenital anomaly of cardiovascular structure of trunk   363028003
  • Congenital anomaly of cerebrovascular system   65587001
  • Congenital anomaly of peripheral blood vessel   430166008
  • Congenital cardiovascular disorder in mother complicating pregnancy, childbirth AND/OR puerperium   6636004
  • Congenital vascular malformation   400159008
  • Levocardia   31420001  removed: 2007-01-31
  • Neonatal Marfan syndrome   763839005
  • Other congenital circulatory system anomalies   204414000  removed: 2010-01-31
  • Other specified circulatory system anomalies   204496004  removed: 2010-01-31
  • Persistent fetal circulation syndrome   35604006  removed: 2019-01-31
  • White forelock with malformations syndrome   763619009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital anomaly of cardiovascular system   9904008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Congenital cardiovascular disorder   762228008
          Congenital anomaly of cardiovascular system   9904008

ancestors
sorted most to least specific
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